Canonical Allele Identifier: CA381583674

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1285624977
• gnomAD v2: 11-67815154-T-C
• gnomAD v4: 11-68047687-T-C
• MyVariant Identifiers: chr11:g.67815154T>C (hg19) ; chr11:g.68047687T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047687T>C , CM000673.2:g.68047687T>C	GRCh38
NC_000011.9:g.67815154T>C , CM000673.1:g.67815154T>C	GRCh37
NC_000011.8:g.67571730T>C	NCBI36
NG_007878.1:g.13672T>C , LRG_115:g.13672T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.875T>C	ENSP00000513629.1:p.Leu292Pro
ENST00000698255.1:c.1295T>C	ENSP00000513630.1:p.Leu432Pro
ENST00000698256.1:c.812T>C
ENST00000698257.1:n.764T>C
ENST00000698258.1:n.404T>C
ENST00000698259.1:n.170T>C
ENST00000265686.8:c.1346T>C MANE Select	ENSP00000265686.3:p.Leu449Pro
ENST00000265686.7:c.1346T>C	ENSP00000265686.3:p.Leu449Pro
ENST00000525516.1:n.140T>C
ENST00000525724.5:n.658T>C
ENST00000528981.5:c.498T>C
ENST00000529364.1:c.757T>C
ENST00000532635.5:c.698T>C	ENSP00000434407.1:p.Leu233Pro
ENST00000533005.5:n.382T>C
NM_006019.3:c.1346T>C	NP_006010.2:p.Leu449Pro
NM_006053.3:c.698T>C	NP_006044.1:p.Leu233Pro
XM_005273709.2:c.1346T>C	XP_005273766.1:p.Leu449Pro
XM_011544726.1:c.1346T>C	XP_011543028.1:p.Leu449Pro
XM_011544727.1:c.1346T>C	XP_011543029.1:p.Leu449Pro
XM_011544728.1:c.1346T>C	XP_011543030.1:p.Leu449Pro
XM_011544729.1:c.1362T>C	XP_011543031.1:p.Ala454=
XR_949754.1:n.1350T>C
NM_001351059.1:c.452T>C	NP_001337988.1:p.Leu151Pro
XM_024448320.1:c.1362T>C	XP_024304088.1:p.Ala454=
XM_024448321.1:c.1362T>C	XP_024304089.1:p.Ala454=
XM_024448322.1:c.1362T>C	XP_024304090.1:p.Ala454=
XM_024448323.1:c.1362T>C	XP_024304091.1:p.Ala454=
XM_024448324.1:c.1362T>C	XP_024304092.1:p.Ala454=
XR_001747721.2:n.1470T>C
XR_001747722.1:n.1483T>C
XR_001747723.2:n.1483T>C
XR_002957115.1:n.1484T>C
NM_006019.4:c.1346T>C MANE Select	NP_006010.2:p.Leu449Pro
NM_001351059.2:c.452T>C	NP_001337988.1:p.Leu151Pro
NM_006053.4:c.698T>C	NP_006044.1:p.Leu233Pro