Canonical Allele Identifier: CA2676181438

Gene: SGCD

Linked Data

• gnomAD v4: 5-156766838-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156766838G>T , CM000667.2:g.156766838G>T	GRCh38
NC_000005.9:g.156193849G>T , CM000667.1:g.156193849G>T	GRCh37
NC_000005.8:g.156126427G>T	NCBI36
NG_008693.2:g.901496G>T , LRG_205:g.901496G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000337851.9:c.*7448G>T MANE Select	ENSP00000338343.4:n.*7448G>T
ENST00000435422.7:c.*7448G>T	ENSP00000403003.2:n.*7448G>T
NM_000337.5:c.*7448G>T , LRG_205t1:c.*7448G>T	NP_000328.2:n.*7448G>T
NM_001128209.1:c.*7448G>T	NP_001121681.1:n.*7448G>T
XM_005265966.3:c.*7448G>T	XP_005266023.1:n.*7448G>T
XM_006714911.2:c.*7448G>T	XP_006714974.1:n.*7448G>T
XM_011534621.1:c.*7448G>T	XP_011532923.1:n.*7448G>T
NM_001128209.2:c.*7448G>T	NP_001121681.1:n.*7448G>T
NM_000337.6:c.*7448G>T MANE Select	NP_000328.2:n.*7448G>T