Canonical Allele Identifier: CA381584552

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815390C>A (hg19) ; chr11:g.68047923C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047923C>A , CM000673.2:g.68047923C>A	GRCh38
NC_000011.9:g.67815390C>A , CM000673.1:g.67815390C>A	GRCh37
NC_000011.8:g.67571966C>A	NCBI36
NG_007878.1:g.13908C>A , LRG_115:g.13908C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.130C>A
ENST00000698254.1:c.1034C>A	ENSP00000513629.1:p.Pro345His
ENST00000698255.1:c.1454C>A	ENSP00000513630.1:p.Pro485His
ENST00000698256.1:c.971C>A
ENST00000698257.1:n.923C>A
ENST00000698258.1:n.640C>A
ENST00000698259.1:n.406C>A
ENST00000265686.8:c.1505C>A MANE Select	ENSP00000265686.3:p.Pro502His
ENST00000265686.7:c.1505C>A	ENSP00000265686.3:p.Pro502His
ENST00000525516.1:n.299C>A
ENST00000525724.5:n.817C>A
ENST00000528981.5:c.657C>A
ENST00000532635.5:c.857C>A	ENSP00000434407.1:p.Pro286His
ENST00000533005.5:n.618C>A
NM_006019.3:c.1505C>A	NP_006010.2:p.Pro502His
NM_006053.3:c.857C>A	NP_006044.1:p.Pro286His
XM_005273709.2:c.1505C>A	XP_005273766.1:p.Pro502His
XM_011544726.1:c.1505C>A	XP_011543028.1:p.Pro502His
XM_011544727.1:c.1505C>A	XP_011543029.1:p.Pro502His
XM_011544728.1:c.1505C>A	XP_011543030.1:p.Pro502His
XR_949754.1:n.1509C>A
NM_001351059.1:c.611C>A	NP_001337988.1:p.Pro204His
XM_024448320.1:c.1598C>A	XP_024304088.1:p.Pro533His
XM_024448321.1:c.1598C>A	XP_024304089.1:p.Pro533His
XM_024448322.1:c.1598C>A	XP_024304090.1:p.Pro533His
XM_024448323.1:c.1598C>A	XP_024304091.1:p.Pro533His
XM_024448324.1:c.1598C>A	XP_024304092.1:p.Pro533His
XR_001747721.2:n.1629C>A
XR_001747722.1:n.1642C>A
XR_001747723.2:n.1642C>A
XR_002957115.1:n.1720C>A
NM_006019.4:c.1505C>A MANE Select	NP_006010.2:p.Pro502His
NM_001351059.2:c.611C>A	NP_001337988.1:p.Pro204His
NM_006053.4:c.857C>A	NP_006044.1:p.Pro286His