Canonical Allele Identifier: CA432386417
Gene: JAGN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.9932478C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9890794C>A , CM000665.2:g.9890794C>A GRCh38
NC_000003.11:g.9932478C>A , CM000665.1:g.9932478C>A GRCh37
NC_000003.10:g.9907478C>A NCBI36
NG_041779.1:g.5208C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000489724.2:c.72C>A ENSP00000497724.1:p.Ala24=
ENST00000647897.1:c.72C>A MANE Select ENSP00000496942.1:p.Ala24=
ENST00000307768.4:c.72C>A ENSP00000306106.4:p.Ala24=
ENST00000489724.1:n.162C>A
ENST00000616966.2:c.72C>A ENSP00000481606.1:p.Ala24=
NM_032492.3:c.72C>A NP_115881.3:p.Ala24=
NM_001363890.1:c.-197C>A NP_001350819.1:n.-197C>A
NM_032492.4:c.72C>A MANE Select NP_115881.3:p.Ala24=