Canonical Allele Identifier: CA381592295

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050664G>A , CM000673.2:g.68050664G>A	GRCh38
NC_000011.9:g.67818131G>A , CM000673.1:g.67818131G>A	GRCh37
NC_000011.8:g.67574707G>A	NCBI36
NG_007878.1:g.16649G>A , LRG_115:g.16649G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2414G>A MANE Select	NP_006010.2:p.Trp805Ter
ENST00000265686.8:c.2414G>A MANE Select	ENSP00000265686.3:p.Trp805Ter
NM_001351059.1:c.1520G>A	NP_001337988.1:p.Trp507Ter
NM_001351059.2:c.1520G>A	NP_001337988.1:p.Trp507Ter
NM_006019.3:c.2414G>A	NP_006010.2:p.Trp805Ter
NM_006053.3:c.1766G>A	NP_006044.1:p.Trp589Ter
NM_006053.4:c.1766G>A	NP_006044.1:p.Trp589Ter
ENST00000265686.7:c.2414G>A	ENSP00000265686.3:p.Trp805Ter
ENST00000525724.5:n.1726G>A
ENST00000530063.1:c.140-77G>A	ENSP00000432957.1:n.140-77G>A
ENST00000530802.1:n.143-77G>A
ENST00000532635.5:c.1766G>A	ENSP00000434407.1:p.Trp589Ter
ENST00000533005.5:n.1527G>A
ENST00000698254.1:c.1943G>A	ENSP00000513629.1:p.Trp648Ter
ENST00000698255.1:c.2363G>A	ENSP00000513630.1:p.Trp788Ter
ENST00000698257.1:n.1832G>A
ENST00000698258.1:n.1549G>A
XM_005273709.2:c.2414G>A	XP_005273766.1:p.Trp805Ter
XM_011544726.1:c.2414G>A	XP_011543028.1:p.Trp805Ter
XM_011544727.1:c.2237-77G>A	XP_011543029.1:n.2237-77G>A
XM_024448320.1:c.2507G>A	XP_024304088.1:p.Trp836Ter
XM_024448321.1:c.2507G>A	XP_024304089.1:p.Trp836Ter
XM_024448322.1:c.2507G>A	XP_024304090.1:p.Trp836Ter
XM_024448323.1:c.2507G>A	XP_024304091.1:p.Trp836Ter
XR_001747721.2:n.2583G>A
XR_001747722.1:n.2551G>A
XR_001747723.2:n.2596G>A
XR_002957115.1:n.2772G>A
XR_949754.1:n.2561G>A