Canonical Allele Identifier: CA1482948014

Gene: GSTCD INTS12

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105767747A= , CM000666.2:g.105767747A=	GRCh38
NC_000004.11:g.106688904A= , CM000666.1:g.106688904A=	GRCh37
NC_000004.10:g.106908353A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370181.1:c.1240+38248A= (GSTCD) MANE Select	NP_001357110.1:n.1240+38248A=
ENST00000515279.6:c.1240+38248A= (GSTCD) MANE Select	ENSP00000422354.1:n.1240+38248A=
NM_001031720.3:c.1240+38248A= (GSTCD)	NP_001026890.2:n.1240+38248A=
NM_024751.3:c.979+38248A= (GSTCD)	NP_079027.2:n.979+38248A=
ENST00000360505.9:c.1240+38248A= (GSTCD)	ENSP00000353695.5:n.1240+38248A=
ENST00000394728.4:c.1240+38248A= (GSTCD)	ENSP00000378216.3:n.1240+38248A=
ENST00000394730.7:c.979+38248A= (GSTCD)	ENSP00000378218.3:n.979+38248A=
ENST00000484843.1:n.1491+38248A= (GSTCD)
ENST00000510876.1:c.31-67733T= (INTS12)	ENSP00000422856.1:n.31-67733T=
ENST00000515255.5:n.579+38248A= (GSTCD)
ENST00000515279.5:c.1240+38248A= (GSTCD)	ENSP00000422354.1:n.1240+38248A=
XM_005263222.2:c.1240+38248A= (GSTCD)	XP_005263279.1:n.1240+38248A=
XM_005263222.4:c.1240+38248A= (GSTCD)	XP_005263279.1:n.1240+38248A=
XM_011532248.1:c.1240+38248A= (GSTCD)	XP_011530550.1:n.1240+38248A=
XM_011532248.3:c.1240+38248A= (GSTCD)	XP_011530550.1:n.1240+38248A=
XM_011532249.1:c.1240+38248A= (GSTCD)	XP_011530551.1:n.1240+38248A=
XM_011532249.3:c.1240+38248A= (GSTCD)	XP_011530551.1:n.1240+38248A=
XM_011532250.1:c.1240+38248A= (GSTCD)	XP_011530552.1:n.1240+38248A=
XM_011532251.1:c.1240+38248A= (GSTCD)	XP_011530553.1:n.1240+38248A=
XM_011532252.1:c.1240+38248A= (GSTCD)	XP_011530554.1:n.1240+38248A=
XM_011532252.3:c.1240+38248A= (GSTCD)	XP_011530554.1:n.1240+38248A=
XR_244687.2:n.1191-14446T=
XR_938771.1:n.1500+38248A= (GSTCD)