Canonical Allele Identifier: CA806117408

Gene: SGCD

Linked Data

• dbSNP Id: rs1208823144
• gnomAD v3: 5-156344417-T-TG
• gnomAD v4: 5-156344417-T-TG
• MyVariant Identifiers: chr5:g.155771427_155771428insG (hg19) ; chr5:g.156344417_156344418insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344417_156344418insG , CM000667.2:g.156344417_156344418insG	GRCh38
NC_000005.9:g.155771427_155771428insG , CM000667.1:g.155771427_155771428insG	GRCh37
NC_000005.8:g.155704005_155704006insG	NCBI36
NG_008693.2:g.479074_479075insG , LRG_205:g.479074_479075insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.4-72_4-71insG MANE Select	ENSP00000338343.4:n.4-72_4-71insG
ENST00000337851.8:c.4-72_4-71insG	ENSP00000338343.4:n.4-72_4-71insG
ENST00000435422.7:c.1-72_1-71insG	ENSP00000403003.2:n.1-72_1-71insG
ENST00000517913.5:c.4-72_4-71insG	ENSP00000429378.1:n.4-72_4-71insG
ENST00000524347.2:c.4-72_4-71insG	ENSP00000430794.1:n.4-72_4-71insG
NM_000337.5:c.4-72_4-71insG , LRG_205t1:c.4-72_4-71insG	NP_000328.2:n.4-72_4-71insG
NM_001128209.1:c.1-72_1-71insG	NP_001121681.1:n.1-72_1-71insG
NM_172244.2:c.4-72_4-71insG	NP_758447.1:n.4-72_4-71insG
XM_005265966.3:c.4-72_4-71insG	XP_005266023.1:n.4-72_4-71insG
XM_005265967.1:c.4-72_4-71insG	XP_005266024.1:n.4-72_4-71insG
XM_006714911.2:c.4-72_4-71insG	XP_006714974.1:n.4-72_4-71insG
XM_011534621.1:c.1-72_1-71insG	XP_011532923.1:n.1-72_1-71insG
XR_941123.1:n.254+3035_254+3036insC
XM_005265966.5:c.4-72_4-71insG	XP_005266023.1:n.4-72_4-71insG
XM_005265967.2:c.4-72_4-71insG	XP_005266024.1:n.4-72_4-71insG
XM_011534621.2:c.1-72_1-71insG	XP_011532923.1:n.1-72_1-71insG
XM_017009723.2:c.4-72_4-71insG	XP_016865212.1:n.4-72_4-71insG
XM_017009724.1:c.4-72_4-71insG	XP_016865213.1:n.4-72_4-71insG
NM_001128209.2:c.1-72_1-71insG	NP_001121681.1:n.1-72_1-71insG
NM_172244.3:c.4-72_4-71insG	NP_758447.1:n.4-72_4-71insG
NM_000337.6:c.4-72_4-71insG MANE Select	NP_000328.2:n.4-72_4-71insG