Canonical Allele Identifier: CA2614697598

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68039764-C-CCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68039765_68039766insAGC , CM000673.2:g.68039765_68039766insAGC	GRCh38
NC_000011.9:g.67807232_67807233insAGC , CM000673.1:g.67807232_67807233insAGC	GRCh37
NC_000011.8:g.67563808_67563809insAGC	NCBI36
NG_007878.1:g.5750_5751insAGC , LRG_115:g.5750_5751insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.-5+646_-5+647insAGC	ENSP00000513629.1:n.-5+646_-5+647insAGC
ENST00000698255.1:c.-5+646_-5+647insAGC	ENSP00000513630.1:n.-5+646_-5+647insAGC
ENST00000265686.8:c.-5+646_-5+647insAGC MANE Select	ENSP00000265686.3:n.-5+646_-5+647insAGC
ENST00000265686.7:c.-5+646_-5+647insAGC	ENSP00000265686.3:n.-5+646_-5+647insAGC
ENST00000524598.5:c.-5+646_-5+647insAGC	ENSP00000432846.1:n.-5+646_-5+647insAGC
ENST00000529657.1:c.-175-27_-175-26insAGC	ENSP00000435023.1:n.-175-27_-175-26insAGC
ENST00000533947.1:n.5+646_5+647insAGC
ENST00000534673.5:c.-5+646_-5+647insAGC	ENSP00000431174.1:n.-5+646_-5+647insAGC
NM_006019.3:c.-5+646_-5+647insAGC	NP_006010.2:n.-5+646_-5+647insAGC
XM_005273709.2:c.-175-27_-175-26insAGC	XP_005273766.1:n.-175-27_-175-26insAGC
NM_001351059.1:c.-1254+646_-1254+647insAGC	NP_001337988.1:n.-1254+646_-1254+647insAGC
XM_024448320.1:c.-5+646_-5+647insAGC	XP_024304088.1:n.-5+646_-5+647insAGC
XM_024448321.1:c.-175-27_-175-26insAGC	XP_024304089.1:n.-175-27_-175-26insAGC
XM_024448323.1:c.-5+646_-5+647insAGC	XP_024304091.1:n.-5+646_-5+647insAGC
XM_024448324.1:c.-5+646_-5+647insAGC	XP_024304092.1:n.-5+646_-5+647insAGC
XR_001747721.2:n.120+646_120+647insAGC
XR_001747722.1:n.117+646_117+647insAGC
XR_001747723.2:n.117+646_117+647insAGC
XR_002957115.1:n.118+646_118+647insAGC
NM_006019.4:c.-5+646_-5+647insAGC MANE Select	NP_006010.2:n.-5+646_-5+647insAGC
NM_001351059.2:c.-1254+646_-1254+647insAGC	NP_001337988.1:n.-1254+646_-1254+647insAGC