Canonical Allele Identifier: CA381592065

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050627G>C , CM000673.2:g.68050627G>C	GRCh38
NC_000011.9:g.67818094G>C , CM000673.1:g.67818094G>C	GRCh37
NC_000011.8:g.67574670G>C	NCBI36
NG_007878.1:g.16612G>C , LRG_115:g.16612G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2377G>C MANE Select	NP_006010.2:p.Gly793Arg
ENST00000265686.8:c.2377G>C MANE Select	ENSP00000265686.3:p.Gly793Arg
NM_001351059.1:c.1483G>C	NP_001337988.1:p.Gly495Arg
NM_001351059.2:c.1483G>C	NP_001337988.1:p.Gly495Arg
NM_006019.3:c.2377G>C	NP_006010.2:p.Gly793Arg
NM_006053.3:c.1729G>C	NP_006044.1:p.Gly577Arg
NM_006053.4:c.1729G>C	NP_006044.1:p.Gly577Arg
ENST00000265686.7:c.2377G>C	ENSP00000265686.3:p.Gly793Arg
ENST00000525724.5:n.1689G>C
ENST00000530063.1:c.140-114G>C	ENSP00000432957.1:n.140-114G>C
ENST00000530449.1:n.505G>C
ENST00000530449.2:n.1602G>C
ENST00000530802.1:n.143-114G>C
ENST00000532635.5:c.1729G>C	ENSP00000434407.1:p.Gly577Arg
ENST00000533005.5:n.1490G>C
ENST00000698254.1:c.1906G>C	ENSP00000513629.1:p.Gly636Arg
ENST00000698255.1:c.2326G>C	ENSP00000513630.1:p.Gly776Arg
ENST00000698257.1:n.1795G>C
ENST00000698258.1:n.1512G>C
XM_005273709.2:c.2377G>C	XP_005273766.1:p.Gly793Arg
XM_011544726.1:c.2377G>C	XP_011543028.1:p.Gly793Arg
XM_011544727.1:c.2237-114G>C	XP_011543029.1:n.2237-114G>C
XM_024448320.1:c.2470G>C	XP_024304088.1:p.Gly824Arg
XM_024448321.1:c.2470G>C	XP_024304089.1:p.Gly824Arg
XM_024448322.1:c.2470G>C	XP_024304090.1:p.Gly824Arg
XM_024448323.1:c.2470G>C	XP_024304091.1:p.Gly824Arg
XR_001747721.2:n.2546G>C
XR_001747722.1:n.2514G>C
XR_001747723.2:n.2559G>C
XR_002957115.1:n.2735G>C
XR_949754.1:n.2524G>C