Canonical Allele Identifier: CA8220582
Community Standard Title: NM_020655.4(JPH3):c.120C>A (p.Thr40=)
Gene: JPH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87603266C>A , CM000678.2:g.87603266C>A GRCh38
NC_000016.9:g.87636872C>A , CM000678.1:g.87636872C>A GRCh37
NC_000016.8:g.86194373C>A NCBI36
NG_009797.1:g.5374C>A

Transcript Alleles

HGVS Amino-acid Change
NM_020655.4:c.120C>A MANE Select NP_065706.2:p.Thr40=
ENST00000284262.3:c.120C>A MANE Select ENSP00000284262.2:p.Thr40=
NM_001271604.2:c.120C>A NP_001258533.1:p.Thr40=
NM_001271604.3:c.120C>A NP_001258533.1:p.Thr40=
NM_001271604.4:c.120C>A NP_001258533.1:p.Thr40=
NM_001271605.1:c.120C>A NP_001258534.1:p.Thr40=
NM_001271605.2:c.120C>A NP_001258534.1:p.Thr40=
NM_001271605.3:c.120C>A NP_001258534.1:p.Thr40=
NM_020655.3:c.120C>A NP_065706.2:p.Thr40=
NR_073379.2:n.96+1336C>A
NR_073379.3:n.96+1336C>A
ENST00000284262.2:c.120C>A ENSP00000284262.2:p.Thr40=
ENST00000301008.5:n.380C>A
ENST00000537256.5:n.96+1336C>A