Canonical Allele Identifier: CA3530679

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156759198T>C , CM000667.2:g.156759198T>C	GRCh38
NC_000005.9:g.156186209T>C , CM000667.1:g.156186209T>C	GRCh37
NC_000005.8:g.156118787T>C	NCBI36
NG_008693.2:g.893856T>C , LRG_205:g.893856T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.700-19T>C MANE Select	ENSP00000338343.4:n.700-19T>C
ENST00000337851.8:c.700-19T>C	ENSP00000338343.4:n.700-19T>C
ENST00000435422.7:c.697-19T>C	ENSP00000403003.2:n.697-19T>C
NM_000337.5:c.700-19T>C , LRG_205t1:c.700-19T>C	NP_000328.2:n.700-19T>C
NM_001128209.1:c.697-19T>C	NP_001121681.1:n.697-19T>C
XM_005265966.3:c.700-19T>C	XP_005266023.1:n.700-19T>C
XM_006714911.2:c.700-19T>C	XP_006714974.1:n.700-19T>C
XM_011534621.1:c.697-19T>C	XP_011532923.1:n.697-19T>C
XM_005265966.5:c.700-19T>C	XP_005266023.1:n.700-19T>C
XM_011534621.2:c.697-19T>C	XP_011532923.1:n.697-19T>C
XM_017009723.2:c.700-19T>C	XP_016865212.1:n.700-19T>C
XM_017009724.1:c.700-19T>C	XP_016865213.1:n.700-19T>C
NM_001128209.2:c.697-19T>C	NP_001121681.1:n.697-19T>C
NM_000337.6:c.700-19T>C MANE Select	NP_000328.2:n.700-19T>C