Canonical Allele Identifier: CA224209433

Gene: TCIRG1

Linked Data

• dbSNP Id: rs374568576
• gnomAD v2: 11-67816363-C-T
• gnomAD v4: 11-68048896-C-T
• MyVariant Identifiers: chr11:g.67816363C>T (hg19) ; chr11:g.68048896C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048896C>T , CM000673.2:g.68048896C>T	GRCh38
NC_000011.9:g.67816363C>T , CM000673.1:g.67816363C>T	GRCh37
NC_000011.8:g.67572939C>T	NCBI36
NG_007878.1:g.14881C>T , LRG_115:g.14881C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.197C>T
ENST00000698254.1:c.1101C>T	ENSP00000513629.1:p.Ala367=
ENST00000698255.1:c.1521C>T	ENSP00000513630.1:p.Ala507=
ENST00000698256.1:c.1038C>T
ENST00000698257.1:n.990C>T
ENST00000698258.1:n.707C>T
ENST00000698259.1:n.473C>T
ENST00000265686.8:c.1572C>T MANE Select	ENSP00000265686.3:p.Ala524=
ENST00000265686.7:c.1572C>T	ENSP00000265686.3:p.Ala524=
ENST00000525724.5:n.884C>T
ENST00000528981.5:c.724C>T
ENST00000532635.5:c.924C>T	ENSP00000434407.1:p.Ala308=
ENST00000533005.5:n.685C>T
NM_006019.3:c.1572C>T	NP_006010.2:p.Ala524=
NM_006053.3:c.924C>T	NP_006044.1:p.Ala308=
XM_005273709.2:c.1572C>T	XP_005273766.1:p.Ala524=
XM_011544726.1:c.1572C>T	XP_011543028.1:p.Ala524=
XM_011544727.1:c.1572C>T	XP_011543029.1:p.Ala524=
XM_011544728.1:c.1572C>T	XP_011543030.1:p.Ala524=
XR_949754.1:n.1576C>T
NM_001351059.1:c.678C>T	NP_001337988.1:p.Ala226=
XM_024448320.1:c.1665C>T	XP_024304088.1:p.Ala555=
XM_024448321.1:c.1665C>T	XP_024304089.1:p.Ala555=
XM_024448322.1:c.1665C>T	XP_024304090.1:p.Ala555=
XM_024448323.1:c.1665C>T	XP_024304091.1:p.Ala555=
XM_024448324.1:c.1665C>T	XP_024304092.1:p.Ala555=
XR_001747721.2:n.1696C>T
XR_001747722.1:n.1709C>T
XR_001747723.2:n.1709C>T
XR_002957115.1:n.1787C>T
NM_006019.4:c.1572C>T MANE Select	NP_006010.2:p.Ala524=
NM_001351059.2:c.678C>T	NP_001337988.1:p.Ala226=
NM_006053.4:c.924C>T	NP_006044.1:p.Ala308=