Canonical Allele Identifier: CA381590182

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050164C>T , CM000673.2:g.68050164C>T	GRCh38
NC_000011.9:g.67817631C>T , CM000673.1:g.67817631C>T	GRCh37
NC_000011.8:g.67574207C>T	NCBI36
NG_007878.1:g.16149C>T , LRG_115:g.16149C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2146C>T MANE Select	NP_006010.2:p.Gln716Ter
ENST00000265686.8:c.2146C>T MANE Select	ENSP00000265686.3:p.Gln716Ter
NM_001351059.1:c.1252C>T	NP_001337988.1:p.Gln418Ter
NM_001351059.2:c.1252C>T	NP_001337988.1:p.Gln418Ter
NM_006019.3:c.2146C>T	NP_006010.2:p.Gln716Ter
NM_006053.3:c.1498C>T	NP_006044.1:p.Gln500Ter
NM_006053.4:c.1498C>T	NP_006044.1:p.Gln500Ter
ENST00000265686.7:c.2146C>T	ENSP00000265686.3:p.Gln716Ter
ENST00000524870.1:n.774C>T
ENST00000525724.5:n.1458C>T
ENST00000530063.1:c.49C>T	ENSP00000432957.1:p.Gln17Ter
ENST00000530449.1:n.42C>T
ENST00000530449.2:n.1139C>T
ENST00000532635.5:c.1498C>T	ENSP00000434407.1:p.Gln500Ter
ENST00000533005.5:n.1259C>T
ENST00000698254.1:c.1675C>T	ENSP00000513629.1:p.Gln559Ter
ENST00000698255.1:c.2095C>T	ENSP00000513630.1:p.Gln699Ter
ENST00000698256.1:c.1612C>T
ENST00000698257.1:n.1564C>T
ENST00000698258.1:n.1281C>T
ENST00000698259.1:n.1415C>T
XM_005273709.2:c.2146C>T	XP_005273766.1:p.Gln716Ter
XM_011544726.1:c.2146C>T	XP_011543028.1:p.Gln716Ter
XM_011544727.1:c.2146C>T	XP_011543029.1:p.Gln716Ter
XM_024448320.1:c.2239C>T	XP_024304088.1:p.Gln747Ter
XM_024448321.1:c.2239C>T	XP_024304089.1:p.Gln747Ter
XM_024448322.1:c.2239C>T	XP_024304090.1:p.Gln747Ter
XM_024448323.1:c.2239C>T	XP_024304091.1:p.Gln747Ter
XR_001747721.2:n.2315C>T
XR_001747722.1:n.2283C>T
XR_001747723.2:n.2328C>T
XR_002957115.1:n.2504C>T
XR_949754.1:n.2293C>T