Canonical Allele Identifier: CA617997001

Gene: SCG3

Linked Data

• dbSNP Id: rs1225899487
• gnomAD v2: 15-51974241-G-GTTTTA
• gnomAD v3: 15-51682044-G-GTTTTA
• gnomAD v4: 15-51682044-G-GTTTTA
• MyVariant Identifiers: chr15:g.51974241_51974242insTTTTA (hg19) ; chr15:g.51682044_51682045insTTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51682046_51682047insTTATT , CM000677.2:g.51682046_51682047insTTATT	GRCh38
NC_000015.9:g.51974243_51974244insTTATT , CM000677.1:g.51974243_51974244insTTATT	GRCh37
NC_000015.8:g.49761535_49761536insTTATT	NCBI36
NG_013214.1:g.5694_5695insTTATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000220478.8:c.82+209_82+210insTTATT MANE Select	ENSP00000220478.3:n.82+209_82+210insTTATT...
ENST00000220478.7:c.82+209_82+210insTTATT	ENSP00000220478.3:n.82+209_82+210insTTATT...
ENST00000542355.6:c.-562+209_-562+210insTTATT	ENSP00000445205.2:n.-562+209_-562+210insT...
ENST00000558709.1:c.-419+209_-419+210insTTATT	ENSP00000452745.1:n.-419+209_-419+210insT...
NM_001165257.1:c.-562+209_-562+210insTTATT	NP_001158729.1:n.-562+209_-562+210insTTAT...
NM_013243.3:c.82+209_82+210insTTATT	NP_037375.2:n.82+209_82+210insTTATT
NM_013243.4:c.82+209_82+210insTTATT MANE Select	NP_037375.2:n.82+209_82+210insTTATT
NM_001165257.2:c.-562+209_-562+210insTTATT	NP_001158729.1:n.-562+209_-562+210insTTAT...