Canonical Allele Identifier: CA1344965536
Gene: JAGN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9890795A= , CM000665.2:g.9890795A= GRCh38
NC_000003.11:g.9932479A= , CM000665.1:g.9932479A= GRCh37
NC_000003.10:g.9907479A= NCBI36
NG_041779.1:g.5209A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000489724.2:c.73A= ENSP00000497724.1:p.Met25=
ENST00000647897.1:c.73A= MANE Select ENSP00000496942.1:p.Met25=
ENST00000307768.4:c.73A= ENSP00000306106.4:p.Met25=
ENST00000489724.1:n.163A=
ENST00000616966.2:c.73A= ENSP00000481606.1:p.Met25=
NM_032492.3:c.73A= NP_115881.3:p.Met25=
NM_001363890.1:c.-196A= NP_001350819.1:n.-196A=
NM_032492.4:c.73A= MANE Select NP_115881.3:p.Met25=