Canonical Allele Identifier: CA381592307

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050665G>T , CM000673.2:g.68050665G>T	GRCh38
NC_000011.9:g.67818132G>T , CM000673.1:g.67818132G>T	GRCh37
NC_000011.8:g.67574708G>T	NCBI36
NG_007878.1:g.16650G>T , LRG_115:g.16650G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2414+1G>T MANE Select	NP_006010.2:n.2414+1G>T
ENST00000265686.8:c.2414+1G>T MANE Select	ENSP00000265686.3:n.2414+1G>T
NM_001351059.1:c.1520+1G>T	NP_001337988.1:n.1520+1G>T
NM_001351059.2:c.1520+1G>T	NP_001337988.1:n.1520+1G>T
NM_006019.3:c.2414+1G>T	NP_006010.2:n.2414+1G>T
NM_006053.3:c.1766+1G>T	NP_006044.1:n.1766+1G>T
NM_006053.4:c.1766+1G>T	NP_006044.1:n.1766+1G>T
ENST00000265686.7:c.2414+1G>T	ENSP00000265686.3:n.2414+1G>T
ENST00000525724.5:n.1726+1G>T
ENST00000530063.1:c.140-76G>T	ENSP00000432957.1:n.140-76G>T
ENST00000530802.1:n.143-76G>T
ENST00000532635.5:c.1766+1G>T	ENSP00000434407.1:n.1766+1G>T
ENST00000533005.5:n.1527+1G>T
ENST00000698254.1:c.1943+1G>T	ENSP00000513629.1:n.1943+1G>T
ENST00000698255.1:c.2363+1G>T	ENSP00000513630.1:n.2363+1G>T
ENST00000698257.1:n.1832+1G>T
ENST00000698258.1:n.1549+1G>T
XM_005273709.2:c.2414+1G>T	XP_005273766.1:n.2414+1G>T
XM_011544726.1:c.2414+1G>T	XP_011543028.1:n.2414+1G>T
XM_011544727.1:c.2237-76G>T	XP_011543029.1:n.2237-76G>T
XM_024448320.1:c.2507+1G>T	XP_024304088.1:n.2507+1G>T
XM_024448321.1:c.2507+1G>T	XP_024304089.1:n.2507+1G>T
XM_024448322.1:c.2507+1G>T	XP_024304090.1:n.2507+1G>T
XM_024448323.1:c.2508G>T	XP_024304091.1:p.Trp836Cys
XR_001747721.2:n.2583+1G>T
XR_001747722.1:n.2551+1G>T
XR_001747723.2:n.2596+1G>T
XR_002957115.1:n.2772+1G>T
XR_949754.1:n.2561+1G>T