Canonical Allele Identifier: CA2695120401

Gene: TAFAZZIN

Linked Data

• gnomAD v4: X-154420783-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420784_154420785del , CM000685.2:g.154420784_154420785del	GRCh38
NC_000023.10:g.153649123_153649124del , CM000685.1:g.153649123_153649124del	GRCh37
NC_000023.9:g.153302317_153302318del	NCBI36
NG_009634.1:g.14247_14248del
NG_009634.2:g.14250_14251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1587+49_1587+50del
ENST00000698317.1:n.2203+49_2203+50del
ENST00000698318.1:n.1986+49_1986+50del
ENST00000698319.1:n.1349+49_1349+50del
ENST00000698320.1:n.1286_1287del
ENST00000470127.2:n.1250+49_1250+50del
ENST00000475699.6:c.741+49_741+50del	ENSP00000419854.3:n.741+49_741+50del
ENST00000483674.3:n.659+49_659+50del
ENST00000601016.6:c.777+49_777+50del MANE Select	ENSP00000469981.1:n.777+49_777+50del
ENST00000612012.5:c.735+49_735+50del	ENSP00000482070.2:n.735+49_735+50del
ENST00000612460.5:c.687+49_687+50del	ENSP00000481037.1:n.687+49_687+50del
ENST00000614595.2:n.2124+49_2124+50del
ENST00000615658.5:n.1366+49_1366+50del
ENST00000616020.5:c.789+49_789+50del	ENSP00000483636.2:n.789+49_789+50del
ENST00000617701.5:c.*790+49_*790+50del	ENSP00000481645.1:n.*790+49_*790+50del
ENST00000651139.1:c.-7+49_-7+50del	ENSP00000498957.1:n.-7+49_-7+50del
ENST00000652354.1:c.459+49_459+50del	ENSP00000498734.1:n.459+49_459+50del
ENST00000652358.1:c.570+49_570+50del	ENSP00000498464.1:n.570+49_570+50del
ENST00000652390.1:c.696+49_696+50del	ENSP00000498858.1:n.696+49_696+50del
ENST00000652476.1:n.1443+49_1443+50del
ENST00000652644.1:c.390+49_390+50del	ENSP00000498496.1:n.390+49_390+50del
ENST00000652682.1:c.834+49_834+50del	ENSP00000498288.1:n.834+49_834+50del
ENST00000652685.1:n.1130+49_1130+50del
ENST00000369776.8:c.687+49_687+50del	ENSP00000358791.4:n.687+49_687+50del
ENST00000426231.5:c.774+49_774+50del
ENST00000475699.5:c.735+49_735+50del	ENSP00000419854.2:n.735+49_735+50del
ENST00000494912.5:n.1466+49_1466+50del
ENST00000498029.1:n.235+49_235+50del
ENST00000601016.5:c.777+49_777+50del	ENSP00000469981.1:n.777+49_777+50del
ENST00000612460.4:c.687+49_687+50del	ENSP00000481037.1:n.687+49_687+50del
ENST00000613002.4:c.645+49_645+50del	ENSP00000478154.1:n.645+49_645+50del
ENST00000615986.4:c.*505+49_*505+50del	ENSP00000480133.1:n.*505+49_*505+50del
NM_000116.4:c.777+49_777+50del	NP_000107.1:n.777+49_777+50del
NM_001303465.1:c.789+49_789+50del	NP_001290394.1:n.789+49_789+50del
NM_181311.3:c.687+49_687+50del	NP_851828.1:n.687+49_687+50del
NM_181312.3:c.735+49_735+50del	NP_851829.1:n.735+49_735+50del
NM_181313.3:c.645+49_645+50del	NP_851830.1:n.645+49_645+50del
NR_024048.2:n.1119+49_1119+50del
XM_006724836.1:c.831+49_831+50del	XP_006724899.1:n.831+49_831+50del
XM_006724837.1:c.816+49_816+50del	XP_006724900.1:n.816+49_816+50del
XM_006724839.1:c.699+49_699+50del	XP_006724902.1:n.699+49_699+50del
XM_006724841.2:c.570+49_570+50del	XP_006724904.1:n.570+49_570+50del
XM_006724842.2:c.480+49_480+50del	XP_006724905.1:n.480+49_480+50del
XM_011531189.1:c.618+49_618+50del	XP_011529491.1:n.618+49_618+50del
XM_011531190.1:c.570+49_570+50del	XP_011529492.1:n.570+49_570+50del
XM_011531191.1:c.501+49_501+50del	XP_011529493.1:n.501+49_501+50del
XM_011531192.1:c.498+49_498+50del	XP_011529494.1:n.498+49_498+50del
XR_938511.1:n.1125+49_1125+50del
XM_006724841.4:c.570+49_570+50del	XP_006724904.1:n.570+49_570+50del
XM_006724842.4:c.480+49_480+50del	XP_006724905.1:n.480+49_480+50del
XM_011531191.2:c.501+49_501+50del	XP_011529493.1:n.501+49_501+50del
XM_017029761.1:c.762+49_762+50del	XP_016885250.1:n.762+49_762+50del
XM_017029762.1:c.741+49_741+50del	XP_016885251.1:n.741+49_741+50del
XM_017029763.1:c.564+49_564+50del	XP_016885252.1:n.564+49_564+50del
XM_017029764.1:c.498+49_498+50del	XP_016885253.1:n.498+49_498+50del
XM_017029765.2:c.438+49_438+50del	XP_016885254.1:n.438+49_438+50del
XM_024452431.1:c.735+49_735+50del	XP_024308199.1:n.735+49_735+50del
NM_000116.5:c.777+49_777+50del MANE Select	NP_000107.1:n.777+49_777+50del
NM_001303465.2:c.789+49_789+50del	NP_001290394.1:n.789+49_789+50del
NM_181311.4:c.687+49_687+50del	NP_851828.1:n.687+49_687+50del
NM_181312.4:c.735+49_735+50del	NP_851829.1:n.735+49_735+50del
NM_181313.4:c.645+49_645+50del	NP_851830.1:n.645+49_645+50del
NR_024048.3:n.1098+49_1098+50del