Canonical Allele Identifier: CA381584475

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67815367G>C (hg19) ; chr11:g.68047900G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047900G>C , CM000673.2:g.68047900G>C	GRCh38
NC_000011.9:g.67815367G>C , CM000673.1:g.67815367G>C	GRCh37
NC_000011.8:g.67571943G>C	NCBI36
NG_007878.1:g.13885G>C , LRG_115:g.13885G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.107G>C
ENST00000698254.1:c.1011G>C	ENSP00000513629.1:p.Gln337His
ENST00000698255.1:c.1431G>C	ENSP00000513630.1:p.Gln477His
ENST00000698256.1:c.948G>C
ENST00000698257.1:n.900G>C
ENST00000698258.1:n.617G>C
ENST00000698259.1:n.383G>C
ENST00000265686.8:c.1482G>C MANE Select	ENSP00000265686.3:p.Gln494His
ENST00000265686.7:c.1482G>C	ENSP00000265686.3:p.Gln494His
ENST00000525516.1:n.276G>C
ENST00000525724.5:n.794G>C
ENST00000528981.5:c.634G>C
ENST00000532635.5:c.834G>C	ENSP00000434407.1:p.Gln278His
ENST00000533005.5:n.595G>C
NM_006019.3:c.1482G>C	NP_006010.2:p.Gln494His
NM_006053.3:c.834G>C	NP_006044.1:p.Gln278His
XM_005273709.2:c.1482G>C	XP_005273766.1:p.Gln494His
XM_011544726.1:c.1482G>C	XP_011543028.1:p.Gln494His
XM_011544727.1:c.1482G>C	XP_011543029.1:p.Gln494His
XM_011544728.1:c.1482G>C	XP_011543030.1:p.Gln494His
XR_949754.1:n.1486G>C
NM_001351059.1:c.588G>C	NP_001337988.1:p.Gln196His
XM_024448320.1:c.1575G>C	XP_024304088.1:p.Gln525His
XM_024448321.1:c.1575G>C	XP_024304089.1:p.Gln525His
XM_024448322.1:c.1575G>C	XP_024304090.1:p.Gln525His
XM_024448323.1:c.1575G>C	XP_024304091.1:p.Gln525His
XM_024448324.1:c.1575G>C	XP_024304092.1:p.Gln525His
XR_001747721.2:n.1606G>C
XR_001747722.1:n.1619G>C
XR_001747723.2:n.1619G>C
XR_002957115.1:n.1697G>C
NM_006019.4:c.1482G>C MANE Select	NP_006010.2:p.Gln494His
NM_001351059.2:c.588G>C	NP_001337988.1:p.Gln196His
NM_006053.4:c.834G>C	NP_006044.1:p.Gln278His