Canonical Allele Identifier: CA362007521

Gene: SGCD

Linked Data

• gnomAD v4: 5-156344502-A-C
• MyVariant Identifiers: chr5:g.155771512A>C (hg19) ; chr5:g.156344502A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344502A>C , CM000667.2:g.156344502A>C	GRCh38
NC_000005.9:g.155771512A>C , CM000667.1:g.155771512A>C	GRCh37
NC_000005.8:g.155704090A>C	NCBI36
NG_008693.2:g.479159A>C , LRG_205:g.479159A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.17A>C MANE Select	ENSP00000338343.4:p.Gln6Pro
ENST00000337851.8:c.17A>C	ENSP00000338343.4:p.Gln6Pro
ENST00000435422.7:c.14A>C	ENSP00000403003.2:p.Gln5Pro
ENST00000517913.5:c.17A>C	ENSP00000429378.1:p.Gln6Pro
ENST00000524347.2:c.17A>C	ENSP00000430794.1:p.Gln6Pro
NM_000337.5:c.17A>C , LRG_205t1:c.17A>C	NP_000328.2:p.Gln6Pro
NM_001128209.1:c.14A>C	NP_001121681.1:p.Gln5Pro
NM_172244.2:c.17A>C	NP_758447.1:p.Gln6Pro
XM_005265966.3:c.17A>C	XP_005266023.1:p.Gln6Pro
XM_005265967.1:c.17A>C	XP_005266024.1:p.Gln6Pro
XM_006714911.2:c.17A>C	XP_006714974.1:p.Gln6Pro
XM_011534621.1:c.14A>C	XP_011532923.1:p.Gln5Pro
XR_941123.1:n.254+2951T>G
XM_005265966.5:c.17A>C	XP_005266023.1:p.Gln6Pro
XM_005265967.2:c.17A>C	XP_005266024.1:p.Gln6Pro
XM_011534621.2:c.14A>C	XP_011532923.1:p.Gln5Pro
XM_017009723.2:c.17A>C	XP_016865212.1:p.Gln6Pro
XM_017009724.1:c.17A>C	XP_016865213.1:p.Gln6Pro
NM_001128209.2:c.14A>C	NP_001121681.1:p.Gln5Pro
NM_172244.3:c.17A>C	NP_758447.1:p.Gln6Pro
NM_000337.6:c.17A>C MANE Select	NP_000328.2:p.Gln6Pro