Canonical Allele Identifier: CA224203244

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68042974C>G , CM000673.2:g.68042974C>G	GRCh38
NC_000011.9:g.67810441C>G , CM000673.1:g.67810441C>G	GRCh37
NC_000011.8:g.67567017C>G	NCBI36
NG_007878.1:g.8959C>G , LRG_115:g.8959C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.446C>G MANE Select	NP_006010.2:p.Ser149Ter
ENST00000265686.8:c.446C>G MANE Select	ENSP00000265686.3:p.Ser149Ter
NM_001351059.1:c.-804C>G	NP_001337988.1:n.-804C>G
NM_001351059.2:c.-804C>G	NP_001337988.1:n.-804C>G
NM_006019.3:c.446C>G	NP_006010.2:p.Ser149Ter
ENST00000265686.7:c.446C>G	ENSP00000265686.3:p.Ser149Ter
ENST00000524598.5:c.404C>G	ENSP00000432846.1:p.Ser135Ter
ENST00000529657.1:c.446C>G	ENSP00000435023.1:p.Ser149Ter
ENST00000533947.1:n.413C>G
ENST00000534673.5:c.446C>G	ENSP00000431174.1:p.Ser149Ter
ENST00000698254.1:c.403+125C>G	ENSP00000513629.1:n.403+125C>G
ENST00000698255.1:c.446C>G	ENSP00000513630.1:p.Ser149Ter
XM_005273709.2:c.446C>G	XP_005273766.1:p.Ser149Ter
XM_011544726.1:c.446C>G	XP_011543028.1:p.Ser149Ter
XM_011544727.1:c.446C>G	XP_011543029.1:p.Ser149Ter
XM_011544728.1:c.446C>G	XP_011543030.1:p.Ser149Ter
XM_011544729.1:c.446C>G	XP_011543031.1:p.Ser149Ter
XM_024448320.1:c.446C>G	XP_024304088.1:p.Ser149Ter
XM_024448321.1:c.446C>G	XP_024304089.1:p.Ser149Ter
XM_024448322.1:c.446C>G	XP_024304090.1:p.Ser149Ter
XM_024448323.1:c.446C>G	XP_024304091.1:p.Ser149Ter
XM_024448324.1:c.446C>G	XP_024304092.1:p.Ser149Ter
XR_001747721.2:n.570C>G
XR_001747722.1:n.567C>G
XR_001747723.2:n.567C>G
XR_002957115.1:n.568C>G
XR_949754.1:n.450C>G