Canonical Allele Identifier: CA713642713
Gene: SCG3 HGNC NCBI

Linked Data

dbSNP Id: rs1348525683
MyVariant Identifiers: chr15:g.51974247_51974248insTGC (hg19) chr15:g.51682050_51682051insTGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51682051_51682052insGCT , CM000677.2:g.51682051_51682052insGCT GRCh38
NC_000015.9:g.51974248_51974249insGCT , CM000677.1:g.51974248_51974249insGCT GRCh37
NC_000015.8:g.49761540_49761541insGCT NCBI36
NG_013214.1:g.5699_5700insGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000220478.8:c.82+214_82+215insGCT MANE Select ENSP00000220478.3:n.82+214_82+215insGCT
ENST00000220478.7:c.82+214_82+215insGCT ENSP00000220478.3:n.82+214_82+215insGCT
ENST00000542355.6:c.-562+214_-562+215insGCT ENSP00000445205.2:n.-562+214_-562+215insGCT
ENST00000558709.1:c.-419+214_-419+215insGCT ENSP00000452745.1:n.-419+214_-419+215insGCT
NM_001165257.1:c.-562+214_-562+215insGCT NP_001158729.1:n.-562+214_-562+215insGCT
NM_013243.3:c.82+214_82+215insGCT NP_037375.2:n.82+214_82+215insGCT
NM_013243.4:c.82+214_82+215insGCT MANE Select NP_037375.2:n.82+214_82+215insGCT
NM_001165257.2:c.-562+214_-562+215insGCT NP_001158729.1:n.-562+214_-562+215insGCT
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