Canonical Allele Identifier: CA1344965543
Gene: JAGN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9890805A= , CM000665.2:g.9890805A= GRCh38
NC_000003.11:g.9932489A= , CM000665.1:g.9932489A= GRCh37
NC_000003.10:g.9907489A= NCBI36
NG_041779.1:g.5219A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000489724.2:c.83A= ENSP00000497724.1:p.Gln28=
ENST00000647897.1:c.83A= MANE Select ENSP00000496942.1:p.Gln28=
ENST00000307768.4:c.83A= ENSP00000306106.4:p.Gln28=
ENST00000489724.1:n.173A=
ENST00000616966.2:c.83A= ENSP00000481606.1:p.Gln28=
NM_032492.3:c.83A= NP_115881.3:p.Gln28=
NM_001363890.1:c.-186A= NP_001350819.1:n.-186A=
NM_032492.4:c.83A= MANE Select NP_115881.3:p.Gln28=