Canonical Allele Identifier: CA362010228

Gene: SGCD

Linked Data

• MyVariant Identifiers: chr5:g.156021951C>T (hg19) ; chr5:g.156594941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156594941C>T , CM000667.2:g.156594941C>T	GRCh38
NC_000005.9:g.156021951C>T , CM000667.1:g.156021951C>T	GRCh37
NC_000005.8:g.155954529C>T	NCBI36
NG_008693.2:g.729598C>T , LRG_205:g.729598C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000337851.9:c.392C>T MANE Select	ENSP00000338343.4:p.Ala131Val
ENST00000337851.8:c.392C>T	ENSP00000338343.4:p.Ala131Val
ENST00000435422.7:c.389C>T	ENSP00000403003.2:p.Ala130Val
ENST00000517913.5:c.392C>T	ENSP00000429378.1:p.Ala131Val
NM_000337.5:c.392C>T , LRG_205t1:c.392C>T	NP_000328.2:p.Ala131Val
NM_001128209.1:c.389C>T	NP_001121681.1:p.Ala130Val
NM_172244.2:c.392C>T	NP_758447.1:p.Ala131Val
XM_005265966.3:c.392C>T	XP_005266023.1:p.Ala131Val
XM_005265967.1:c.392C>T	XP_005266024.1:p.Ala131Val
XM_006714911.2:c.392C>T	XP_006714974.1:p.Ala131Val
XM_011534621.1:c.389C>T	XP_011532923.1:p.Ala130Val
XM_005265966.5:c.392C>T	XP_005266023.1:p.Ala131Val
XM_005265967.2:c.392C>T	XP_005266024.1:p.Ala131Val
XM_011534621.2:c.389C>T	XP_011532923.1:p.Ala130Val
XM_017009723.2:c.392C>T	XP_016865212.1:p.Ala131Val
XM_017009724.1:c.392C>T	XP_016865213.1:p.Ala131Val
NM_001128209.2:c.389C>T	NP_001121681.1:p.Ala130Val
NM_172244.3:c.392C>T	NP_758447.1:p.Ala131Val
NM_000337.6:c.392C>T MANE Select	NP_000328.2:p.Ala131Val