Canonical Allele Identifier: CA362007535

Gene: SGCD

Linked Data

• gnomAD v4: 5-156344507-A-T
• MyVariant Identifiers: chr5:g.155771517A>T (hg19) ; chr5:g.156344507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344507A>T , CM000667.2:g.156344507A>T	GRCh38
NC_000005.9:g.155771517A>T , CM000667.1:g.155771517A>T	GRCh37
NC_000005.8:g.155704095A>T	NCBI36
NG_008693.2:g.479164A>T , LRG_205:g.479164A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.22A>T MANE Select	ENSP00000338343.4:p.Thr8Ser
ENST00000337851.8:c.22A>T	ENSP00000338343.4:p.Thr8Ser
ENST00000435422.7:c.19A>T	ENSP00000403003.2:p.Thr7Ser
ENST00000517913.5:c.22A>T	ENSP00000429378.1:p.Thr8Ser
ENST00000524347.2:c.22A>T	ENSP00000430794.1:p.Thr8Ser
NM_000337.5:c.22A>T , LRG_205t1:c.22A>T	NP_000328.2:p.Thr8Ser
NM_001128209.1:c.19A>T	NP_001121681.1:p.Thr7Ser
NM_172244.2:c.22A>T	NP_758447.1:p.Thr8Ser
XM_005265966.3:c.22A>T	XP_005266023.1:p.Thr8Ser
XM_005265967.1:c.22A>T	XP_005266024.1:p.Thr8Ser
XM_006714911.2:c.22A>T	XP_006714974.1:p.Thr8Ser
XM_011534621.1:c.19A>T	XP_011532923.1:p.Thr7Ser
XR_941123.1:n.254+2946T>A
XM_005265966.5:c.22A>T	XP_005266023.1:p.Thr8Ser
XM_005265967.2:c.22A>T	XP_005266024.1:p.Thr8Ser
XM_011534621.2:c.19A>T	XP_011532923.1:p.Thr7Ser
XM_017009723.2:c.22A>T	XP_016865212.1:p.Thr8Ser
XM_017009724.1:c.22A>T	XP_016865213.1:p.Thr8Ser
NM_001128209.2:c.19A>T	NP_001121681.1:p.Thr7Ser
NM_172244.3:c.22A>T	NP_758447.1:p.Thr8Ser
NM_000337.6:c.22A>T MANE Select	NP_000328.2:p.Thr8Ser