Canonical Allele Identifier: CA1344965582
Gene: JAGN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9890860T= , CM000665.2:g.9890860T= GRCh38
NC_000003.11:g.9932544T= , CM000665.1:g.9932544T= GRCh37
NC_000003.10:g.9907544T= NCBI36
NG_041779.1:g.5274T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000489724.2:c.89+49T= ENSP00000497724.1:n.89+49T=
ENST00000647897.1:c.89+49T= MANE Select ENSP00000496942.1:n.89+49T=
ENST00000307768.4:c.89+49T= ENSP00000306106.4:n.89+49T=
ENST00000489724.1:n.179+49T=
ENST00000616966.2:c.89+49T= ENSP00000481606.1:n.89+49T=
NM_032492.3:c.89+49T= NP_115881.3:n.89+49T=
NM_001363890.1:c.-180+49T= NP_001350819.1:n.-180+49T=
NM_032492.4:c.89+49T= MANE Select NP_115881.3:n.89+49T=