Canonical Allele Identifier: CA381584547

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815389C>A (hg19) ; chr11:g.68047922C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047922C>A , CM000673.2:g.68047922C>A	GRCh38
NC_000011.9:g.67815389C>A , CM000673.1:g.67815389C>A	GRCh37
NC_000011.8:g.67571965C>A	NCBI36
NG_007878.1:g.13907C>A , LRG_115:g.13907C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.129C>A
ENST00000698254.1:c.1033C>A	ENSP00000513629.1:p.Pro345Thr
ENST00000698255.1:c.1453C>A	ENSP00000513630.1:p.Pro485Thr
ENST00000698256.1:c.970C>A
ENST00000698257.1:n.922C>A
ENST00000698258.1:n.639C>A
ENST00000698259.1:n.405C>A
ENST00000265686.8:c.1504C>A MANE Select	ENSP00000265686.3:p.Pro502Thr
ENST00000265686.7:c.1504C>A	ENSP00000265686.3:p.Pro502Thr
ENST00000525516.1:n.298C>A
ENST00000525724.5:n.816C>A
ENST00000528981.5:c.656C>A
ENST00000532635.5:c.856C>A	ENSP00000434407.1:p.Pro286Thr
ENST00000533005.5:n.617C>A
NM_006019.3:c.1504C>A	NP_006010.2:p.Pro502Thr
NM_006053.3:c.856C>A	NP_006044.1:p.Pro286Thr
XM_005273709.2:c.1504C>A	XP_005273766.1:p.Pro502Thr
XM_011544726.1:c.1504C>A	XP_011543028.1:p.Pro502Thr
XM_011544727.1:c.1504C>A	XP_011543029.1:p.Pro502Thr
XM_011544728.1:c.1504C>A	XP_011543030.1:p.Pro502Thr
XR_949754.1:n.1508C>A
NM_001351059.1:c.610C>A	NP_001337988.1:p.Pro204Thr
XM_024448320.1:c.1597C>A	XP_024304088.1:p.Pro533Thr
XM_024448321.1:c.1597C>A	XP_024304089.1:p.Pro533Thr
XM_024448322.1:c.1597C>A	XP_024304090.1:p.Pro533Thr
XM_024448323.1:c.1597C>A	XP_024304091.1:p.Pro533Thr
XM_024448324.1:c.1597C>A	XP_024304092.1:p.Pro533Thr
XR_001747721.2:n.1628C>A
XR_001747722.1:n.1641C>A
XR_001747723.2:n.1641C>A
XR_002957115.1:n.1719C>A
NM_006019.4:c.1504C>A MANE Select	NP_006010.2:p.Pro502Thr
NM_001351059.2:c.610C>A	NP_001337988.1:p.Pro204Thr
NM_006053.4:c.856C>A	NP_006044.1:p.Pro286Thr