Canonical Allele Identifier: CA6146780

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043654G>T , CM000673.2:g.68043654G>T	GRCh38
NC_000011.9:g.67811121G>T , CM000673.1:g.67811121G>T	GRCh37
NC_000011.8:g.67567697G>T	NCBI36
NG_007878.1:g.9639G>T , LRG_115:g.9639G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.713+1G>T MANE Select	NP_006010.2:n.713+1G>T
ENST00000265686.8:c.713+1G>T MANE Select	ENSP00000265686.3:n.713+1G>T
NM_001351059.1:c.-198+1G>T	NP_001337988.1:n.-198+1G>T
NM_001351059.2:c.-198+1G>T	NP_001337988.1:n.-198+1G>T
NM_006019.3:c.713+1G>T	NP_006010.2:n.713+1G>T
NM_006053.3:c.65+1G>T	NP_006044.1:n.65+1G>T
NM_006053.4:c.65+1G>T	NP_006044.1:n.65+1G>T
ENST00000265686.7:c.713+1G>T	ENSP00000265686.3:n.713+1G>T
ENST00000524598.5:c.671+1G>T	ENSP00000432846.1:n.671+1G>T
ENST00000527530.1:n.331+1G>T
ENST00000529364.1:c.213+1G>T
ENST00000532635.5:c.65+1G>T	ENSP00000434407.1:n.65+1G>T
ENST00000534673.5:c.*61+1G>T	ENSP00000431174.1:n.*61+1G>T
ENST00000698254.1:c.404-545G>T	ENSP00000513629.1:n.404-545G>T
ENST00000698255.1:c.662+1G>T	ENSP00000513630.1:n.662+1G>T
ENST00000698256.1:c.163+1G>T
ENST00000698257.1:n.131+1G>T
XM_005273709.2:c.713+1G>T	XP_005273766.1:n.713+1G>T
XM_011544726.1:c.713+1G>T	XP_011543028.1:n.713+1G>T
XM_011544727.1:c.713+1G>T	XP_011543029.1:n.713+1G>T
XM_011544728.1:c.713+1G>T	XP_011543030.1:n.713+1G>T
XM_011544729.1:c.713+1G>T	XP_011543031.1:n.713+1G>T
XM_024448320.1:c.713+1G>T	XP_024304088.1:n.713+1G>T
XM_024448321.1:c.713+1G>T	XP_024304089.1:n.713+1G>T
XM_024448322.1:c.713+1G>T	XP_024304090.1:n.713+1G>T
XM_024448323.1:c.713+1G>T	XP_024304091.1:n.713+1G>T
XM_024448324.1:c.713+1G>T	XP_024304092.1:n.713+1G>T
XR_001747721.2:n.837+1G>T
XR_001747722.1:n.834+1G>T
XR_001747723.2:n.834+1G>T
XR_002957115.1:n.835+1G>T
XR_949754.1:n.717+1G>T