Canonical Allele Identifier: CA806117393

Gene: SGCD

Linked Data

• dbSNP Id: rs80276463
• gnomAD v3: 5-156344411-AT-A
• gnomAD v4: 5-156344411-AT-A
• MyVariant Identifiers: chr5:g.155771422del (hg19) ; chr5:g.156344412del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.156344420del , CM000667.2:g.156344420del	GRCh38
NC_000005.9:g.155771430del , CM000667.1:g.155771430del	GRCh37
NC_000005.8:g.155704008del	NCBI36
NG_008693.2:g.479077del , LRG_205:g.479077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337851.9:c.4-69del MANE Select	ENSP00000338343.4:n.4-69del
ENST00000337851.8:c.4-69del	ENSP00000338343.4:n.4-69del
ENST00000435422.7:c.1-69del	ENSP00000403003.2:n.1-69del
ENST00000517913.5:c.4-69del	ENSP00000429378.1:n.4-69del
ENST00000524347.2:c.4-69del	ENSP00000430794.1:n.4-69del
NM_000337.5:c.4-69del , LRG_205t1:c.4-69del	NP_000328.2:n.4-69del
NM_001128209.1:c.1-69del	NP_001121681.1:n.1-69del
NM_172244.2:c.4-69del	NP_758447.1:n.4-69del
XM_005265966.3:c.4-69del	XP_005266023.1:n.4-69del
XM_005265967.1:c.4-69del	XP_005266024.1:n.4-69del
XM_006714911.2:c.4-69del	XP_006714974.1:n.4-69del
XM_011534621.1:c.1-69del	XP_011532923.1:n.1-69del
XR_941123.1:n.254+3041del
XM_005265966.5:c.4-69del	XP_005266023.1:n.4-69del
XM_005265967.2:c.4-69del	XP_005266024.1:n.4-69del
XM_011534621.2:c.1-69del	XP_011532923.1:n.1-69del
XM_017009723.2:c.4-69del	XP_016865212.1:n.4-69del
XM_017009724.1:c.4-69del	XP_016865213.1:n.4-69del
NM_001128209.2:c.1-69del	NP_001121681.1:n.1-69del
NM_172244.3:c.4-69del	NP_758447.1:n.4-69del
NM_000337.6:c.4-69del MANE Select	NP_000328.2:n.4-69del