Canonical Allele Identifier: CA2532753204

Gene: SGCD

Linked Data

• gnomAD v4: 5-156329538-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156329538A>G , CM000667.2:g.156329538A>G	GRCh38
NC_000005.9:g.155756548A>G , CM000667.1:g.155756548A>G	GRCh37
NC_000005.8:g.155689126A>G	NCBI36
NG_008693.2:g.464195A>G , LRG_205:g.464195A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000337851.9:c.-39A>G MANE Select	ENSP00000338343.4:n.-39A>G
ENST00000337851.8:c.-39A>G	ENSP00000338343.4:n.-39A>G
ENST00000435422.7:c.-1+2306A>G	ENSP00000403003.2:n.-1+2306A>G
ENST00000517913.5:c.-39A>G	ENSP00000429378.1:n.-39A>G
ENST00000524347.2:c.-39A>G	ENSP00000430794.1:n.-39A>G
NM_000337.5:c.-39A>G , LRG_205t1:c.-39A>G	NP_000328.2:n.-39A>G
NM_001128209.1:c.-1+2306A>G	NP_001121681.1:n.-1+2306A>G
NM_172244.2:c.-39A>G	NP_758447.1:n.-39A>G
XM_005265966.3:c.-39A>G	XP_005266023.1:n.-39A>G
XM_005265967.1:c.-39A>G	XP_005266024.1:n.-39A>G
XM_006714911.2:c.-39A>G	XP_006714974.1:n.-39A>G
XM_011534621.1:c.1-14951A>G	XP_011532923.1:n.1-14951A>G
XR_941123.1:n.254+17915T>C
XM_005265966.5:c.-39A>G	XP_005266023.1:n.-39A>G
XM_005265967.2:c.-39A>G	XP_005266024.1:n.-39A>G
XM_011534621.2:c.1-14951A>G	XP_011532923.1:n.1-14951A>G
XM_017009723.2:c.-39A>G	XP_016865212.1:n.-39A>G
XM_017009724.1:c.-39A>G	XP_016865213.1:n.-39A>G
NM_001128209.2:c.-1+2306A>G	NP_001121681.1:n.-1+2306A>G
NM_172244.3:c.-39A>G	NP_758447.1:n.-39A>G
NM_000337.6:c.-39A>G MANE Select	NP_000328.2:n.-39A>G