Canonical Allele Identifier: CA3530697

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156759309C>T , CM000667.2:g.156759309C>T	GRCh38
NC_000005.9:g.156186320C>T , CM000667.1:g.156186320C>T	GRCh37
NC_000005.8:g.156118898C>T	NCBI36
NG_008693.2:g.893967C>T , LRG_205:g.893967C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000337.6:c.792C>T MANE Select	NP_000328.2:p.Cys264=
ENST00000337851.9:c.792C>T MANE Select	ENSP00000338343.4:p.Cys264=
NM_000337.5:c.792C>T , LRG_205t1:c.792C>T	NP_000328.2:p.Cys264=
NM_001128209.1:c.789C>T	NP_001121681.1:p.Cys263=
NM_001128209.2:c.789C>T	NP_001121681.1:p.Cys263=
ENST00000337851.8:c.792C>T	ENSP00000338343.4:p.Cys264=
ENST00000435422.7:c.789C>T	ENSP00000403003.2:p.Cys263=
XM_005265966.3:c.792C>T	XP_005266023.1:p.Cys264=
XM_005265966.5:c.792C>T	XP_005266023.1:p.Cys264=
XM_006714911.2:c.792C>T	XP_006714974.1:p.Cys264=
XM_011534621.1:c.789C>T	XP_011532923.1:p.Cys263=
XM_011534621.2:c.789C>T	XP_011532923.1:p.Cys263=
XM_017009723.2:c.792C>T	XP_016865212.1:p.Cys264=
XM_017009724.1:c.792C>T	XP_016865213.1:p.Cys264=