Canonical Allele Identifier: CA381580542

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044251C>A , CM000673.2:g.68044251C>A	GRCh38
NC_000011.9:g.67811718C>A , CM000673.1:g.67811718C>A	GRCh37
NC_000011.8:g.67568294C>A	NCBI36
NG_007878.1:g.10236C>A , LRG_115:g.10236C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.927C>A MANE Select	NP_006010.2:p.Cys309Ter
ENST00000265686.8:c.927C>A MANE Select	ENSP00000265686.3:p.Cys309Ter
NM_001351059.1:c.33C>A	NP_001337988.1:p.Cys11Ter
NM_001351059.2:c.33C>A	NP_001337988.1:p.Cys11Ter
NM_006019.3:c.927C>A	NP_006010.2:p.Cys309Ter
NM_006053.3:c.279C>A	NP_006044.1:p.Cys93Ter
NM_006053.4:c.279C>A	NP_006044.1:p.Cys93Ter
ENST00000265686.7:c.927C>A	ENSP00000265686.3:p.Cys309Ter
ENST00000524598.5:c.885C>A	ENSP00000432846.1:p.Cys295Ter
ENST00000525724.5:n.239C>A
ENST00000528981.5:c.17C>A
ENST00000529364.1:c.427C>A
ENST00000532635.5:c.279C>A	ENSP00000434407.1:p.Cys93Ter
ENST00000698254.1:c.456C>A	ENSP00000513629.1:p.Cys152Ter
ENST00000698255.1:c.876C>A	ENSP00000513630.1:p.Cys292Ter
ENST00000698256.1:c.393C>A
ENST00000698257.1:n.345C>A
XM_005273709.2:c.927C>A	XP_005273766.1:p.Cys309Ter
XM_011544726.1:c.927C>A	XP_011543028.1:p.Cys309Ter
XM_011544727.1:c.927C>A	XP_011543029.1:p.Cys309Ter
XM_011544728.1:c.927C>A	XP_011543030.1:p.Cys309Ter
XM_011544729.1:c.943C>A	XP_011543031.1:p.Gln315Lys
XM_024448320.1:c.943C>A	XP_024304088.1:p.Gln315Lys
XM_024448321.1:c.943C>A	XP_024304089.1:p.Gln315Lys
XM_024448322.1:c.943C>A	XP_024304090.1:p.Gln315Lys
XM_024448323.1:c.943C>A	XP_024304091.1:p.Gln315Lys
XM_024448324.1:c.943C>A	XP_024304092.1:p.Gln315Lys
XR_001747721.2:n.1051C>A
XR_001747722.1:n.1064C>A
XR_001747723.2:n.1064C>A
XR_002957115.1:n.1065C>A
XR_949754.1:n.931C>A