Canonical Allele Identifier: CA2520913724

Gene: SGCD

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344401_156344402insTGG , CM000667.2:g.156344401_156344402insTGG	GRCh38
NC_000005.9:g.155771411_155771412insTGG , CM000667.1:g.155771411_155771412insTGG	GRCh37
NC_000005.8:g.155703989_155703990insTGG	NCBI36
NG_008693.2:g.479058_479059insTGG , LRG_205:g.479058_479059insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.4-88_4-87insTGG MANE Select	ENSP00000338343.4:n.4-88_4-87insTGG
ENST00000337851.8:c.4-88_4-87insTGG	ENSP00000338343.4:n.4-88_4-87insTGG
ENST00000435422.7:c.1-88_1-87insTGG	ENSP00000403003.2:n.1-88_1-87insTGG
ENST00000517913.5:c.4-88_4-87insTGG	ENSP00000429378.1:n.4-88_4-87insTGG
ENST00000524347.2:c.4-88_4-87insTGG	ENSP00000430794.1:n.4-88_4-87insTGG
NM_000337.5:c.4-88_4-87insTGG , LRG_205t1:c.4-88_4-87insTGG	NP_000328.2:n.4-88_4-87insTGG
NM_001128209.1:c.1-88_1-87insTGG	NP_001121681.1:n.1-88_1-87insTGG
NM_172244.2:c.4-88_4-87insTGG	NP_758447.1:n.4-88_4-87insTGG
XM_005265966.3:c.4-88_4-87insTGG	XP_005266023.1:n.4-88_4-87insTGG
XM_005265967.1:c.4-88_4-87insTGG	XP_005266024.1:n.4-88_4-87insTGG
XM_006714911.2:c.4-88_4-87insTGG	XP_006714974.1:n.4-88_4-87insTGG
XM_011534621.1:c.1-88_1-87insTGG	XP_011532923.1:n.1-88_1-87insTGG
XR_941123.1:n.254+3051_254+3052insCCA
XM_005265966.5:c.4-88_4-87insTGG	XP_005266023.1:n.4-88_4-87insTGG
XM_005265967.2:c.4-88_4-87insTGG	XP_005266024.1:n.4-88_4-87insTGG
XM_011534621.2:c.1-88_1-87insTGG	XP_011532923.1:n.1-88_1-87insTGG
XM_017009723.2:c.4-88_4-87insTGG	XP_016865212.1:n.4-88_4-87insTGG
XM_017009724.1:c.4-88_4-87insTGG	XP_016865213.1:n.4-88_4-87insTGG
NM_001128209.2:c.1-88_1-87insTGG	NP_001121681.1:n.1-88_1-87insTGG
NM_172244.3:c.4-88_4-87insTGG	NP_758447.1:n.4-88_4-87insTGG
NM_000337.6:c.4-88_4-87insTGG MANE Select	NP_000328.2:n.4-88_4-87insTGG