Canonical Allele Identifier: CA381584539

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815387A>C (hg19) ; chr11:g.68047920A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047920A>C , CM000673.2:g.68047920A>C	GRCh38
NC_000011.9:g.67815387A>C , CM000673.1:g.67815387A>C	GRCh37
NC_000011.8:g.67571963A>C	NCBI36
NG_007878.1:g.13905A>C , LRG_115:g.13905A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.127A>C
ENST00000698254.1:c.1031A>C	ENSP00000513629.1:p.Asp344Ala
ENST00000698255.1:c.1451A>C	ENSP00000513630.1:p.Asp484Ala
ENST00000698256.1:c.968A>C
ENST00000698257.1:n.920A>C
ENST00000698258.1:n.637A>C
ENST00000698259.1:n.403A>C
ENST00000265686.8:c.1502A>C MANE Select	ENSP00000265686.3:p.Asp501Ala
ENST00000265686.7:c.1502A>C	ENSP00000265686.3:p.Asp501Ala
ENST00000525516.1:n.296A>C
ENST00000525724.5:n.814A>C
ENST00000528981.5:c.654A>C
ENST00000532635.5:c.854A>C	ENSP00000434407.1:p.Asp285Ala
ENST00000533005.5:n.615A>C
NM_006019.3:c.1502A>C	NP_006010.2:p.Asp501Ala
NM_006053.3:c.854A>C	NP_006044.1:p.Asp285Ala
XM_005273709.2:c.1502A>C	XP_005273766.1:p.Asp501Ala
XM_011544726.1:c.1502A>C	XP_011543028.1:p.Asp501Ala
XM_011544727.1:c.1502A>C	XP_011543029.1:p.Asp501Ala
XM_011544728.1:c.1502A>C	XP_011543030.1:p.Asp501Ala
XR_949754.1:n.1506A>C
NM_001351059.1:c.608A>C	NP_001337988.1:p.Asp203Ala
XM_024448320.1:c.1595A>C	XP_024304088.1:p.Asp532Ala
XM_024448321.1:c.1595A>C	XP_024304089.1:p.Asp532Ala
XM_024448322.1:c.1595A>C	XP_024304090.1:p.Asp532Ala
XM_024448323.1:c.1595A>C	XP_024304091.1:p.Asp532Ala
XM_024448324.1:c.1595A>C	XP_024304092.1:p.Asp532Ala
XR_001747721.2:n.1626A>C
XR_001747722.1:n.1639A>C
XR_001747723.2:n.1639A>C
XR_002957115.1:n.1717A>C
NM_006019.4:c.1502A>C MANE Select	NP_006010.2:p.Asp501Ala
NM_001351059.2:c.608A>C	NP_001337988.1:p.Asp203Ala
NM_006053.4:c.854A>C	NP_006044.1:p.Asp285Ala