Canonical Allele Identifier: CA1675959620

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115141_158115145delinsCACTT , CM000668.2:g.158115141_158115145delinsCACTT	GRCh38
NC_000006.11:g.158536173_158536177delinsCACTT , CM000668.1:g.158536173_158536177delinsCACTT	GRCh37
NC_000006.10:g.158456161_158456165delinsCACTT	NCBI36
NG_032889.1:g.58136_58140delinsAAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-174_714-170delinsAAGTG	ENSP00000391168.2:n.714-174_714-170delinsAAGTG
ENST00000607071.6:c.*1222-174_*1222-170delinsAAGTG	ENSP00000475855.1:n.*1222-174_*1222-170delinsAAGTG
ENST00000642244.1:c.1412-174_1412-170delinsAAGTG	ENSP00000493554.1:n.1412-174_1412-170delinsAAGTG
ENST00000642903.1:c.1502-174_1502-170delinsAAGTG	ENSP00000493559.1:n.1502-174_1502-170delinsAAGTG
ENST00000644972.1:c.1502-174_1502-170delinsAAGTG	ENSP00000496451.1:n.1502-174_1502-170delinsAAGTG
ENST00000645077.1:c.*1123-174_*1123-170delinsAAGTG	ENSP00000496113.1:n.*1123-174_*1123-170delinsAAGTG
ENST00000645172.1:c.*1204-174_*1204-170delinsAAGTG	ENSP00000495367.1:n.*1204-174_*1204-170delinsAAGTG
ENST00000646190.1:n.2833-174_2833-170delinsAAGTG
ENST00000646208.1:c.1238-174_1238-170delinsAAGTG	ENSP00000493723.1:n.1238-174_1238-170delinsAAGTG
ENST00000646410.1:c.1373-174_1373-170delinsAAGTG	ENSP00000494205.1:n.1373-174_1373-170delinsAAGTG
ENST00000646562.1:c.*1336-174_*1336-170delinsAAGTG	ENSP00000496087.1:n.*1336-174_*1336-170delinsAAGTG
ENST00000647468.2:c.1502-174_1502-170delinsAAGTG MANE Select	ENSP00000496731.1:n.1502-174_1502-170delinsAAGTG
ENST00000648111.1:c.*1190-174_*1190-170delinsAAGTG	ENSP00000497275.1:n.*1190-174_*1190-170delinsAAGTG
ENST00000367101.5:c.1546-174_1546-170delinsAAGTG	ENSP00000356068.1:n.1546-174_1546-170delinsAAGTG
ENST00000367104.7:c.1502-174_1502-170delinsAAGTG	ENSP00000356071.3:n.1502-174_1502-170delinsAAGTG
ENST00000435180.5:c.227-174_227-170delinsAAGTG	ENSP00000391168.1:n.227-174_227-170delinsAAGTG
ENST00000606965.5:c.*63-174_*63-170delinsAAGTG	ENSP00000475808.1:n.*63-174_*63-170delinsAAGTG
ENST00000607071.5:c.*1436-174_*1436-170delinsAAGTG	ENSP00000475855.1:n.*1436-174_*1436-170delinsAAGTG
ENST00000607742.5:c.*2780-174_*2780-170delinsAAGTG	ENSP00000475523.1:n.*2780-174_*2780-170delinsAAGTG
NM_032861.3:c.1502-174_1502-170delinsAAGTG	NP_116250.3:n.1502-174_1502-170delinsAAGTG
NR_073096.1:n.1435-174_1435-170delinsAAGTG
XM_006715586.1:c.1292-174_1292-170delinsAAGTG	XP_006715649.1:n.1292-174_1292-170delinsAAGTG
XM_011536196.1:c.1481-174_1481-170delinsAAGTG	XP_011534498.1:n.1481-174_1481-170delinsAAGTG
XM_011536197.1:c.1388-174_1388-170delinsAAGTG	XP_011534499.1:n.1388-174_1388-170delinsAAGTG
XM_011536198.1:c.1292-174_1292-170delinsAAGTG	XP_011534500.1:n.1292-174_1292-170delinsAAGTG
XM_006715586.3:c.1292-174_1292-170delinsAAGTG	XP_006715649.1:n.1292-174_1292-170delinsAAGTG
XM_011536196.3:c.1481-174_1481-170delinsAAGTG	XP_011534498.1:n.1481-174_1481-170delinsAAGTG
XM_011536198.3:c.1292-174_1292-170delinsAAGTG	XP_011534500.1:n.1292-174_1292-170delinsAAGTG
XM_024446573.1:c.1502-174_1502-170delinsAAGTG	XP_024302341.1:n.1502-174_1502-170delinsAAGTG
XR_001743697.2:n.1533-174_1533-170delinsAAGTG
XR_942606.2:n.1584-174_1584-170delinsAAGTG
NM_032861.4:c.1502-174_1502-170delinsAAGTG MANE Select	NP_116250.3:n.1502-174_1502-170delinsAAGTG
NR_073096.2:n.1417-174_1417-170delinsAAGTG