Canonical Allele Identifier: CA806144344

Gene: SGCD

Linked Data

• dbSNP Id: rs1281758654
• MyVariant Identifiers: chr5:g.156181875del (hg19) ; chr5:g.156754864del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156754865del , CM000667.2:g.156754865del	GRCh38
NC_000005.9:g.156181876del , CM000667.1:g.156181876del	GRCh37
NC_000005.8:g.156114454del	NCBI36
NG_008693.2:g.889523del , LRG_205:g.889523del

Transcript Alleles

HGVS	Amino-acid change
ENST00000337851.9:c.576-2716del MANE Select	ENSP00000338343.4:n.576-2716del
ENST00000337851.8:c.576-2716del	ENSP00000338343.4:n.576-2716del
ENST00000435422.7:c.573-2716del	ENSP00000403003.2:n.573-2716del
ENST00000517913.5:c.576-2716del	ENSP00000429378.1:n.576-2716del
NM_000337.5:c.576-2716del , LRG_205t1:c.576-2716del	NP_000328.2:n.576-2716del
NM_001128209.1:c.573-2716del	NP_001121681.1:n.573-2716del
NM_172244.2:c.576-2716del	NP_758447.1:n.576-2716del
XM_005265966.3:c.576-2716del	XP_005266023.1:n.576-2716del
XM_005265967.1:c.503-2716del	XP_005266024.1:n.503-2716del
XM_006714911.2:c.576-2716del	XP_006714974.1:n.576-2716del
XM_011534621.1:c.573-2716del	XP_011532923.1:n.573-2716del
XM_005265966.5:c.576-2716del	XP_005266023.1:n.576-2716del
XM_005265967.2:c.503-2716del	XP_005266024.1:n.503-2716del
XM_011534621.2:c.573-2716del	XP_011532923.1:n.573-2716del
XM_017009723.2:c.576-2716del	XP_016865212.1:n.576-2716del
XM_017009724.1:c.576-2716del	XP_016865213.1:n.576-2716del
NM_001128209.2:c.573-2716del	NP_001121681.1:n.573-2716del
NM_172244.3:c.576-2716del	NP_758447.1:n.576-2716del
NM_000337.6:c.576-2716del MANE Select	NP_000328.2:n.576-2716del