Canonical Allele Identifier: CA2326737219
Gene: NCAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19219016T= , CM000681.2:g.19219016T= GRCh38
NC_000019.9:g.19329825T= , CM000681.1:g.19329825T= GRCh37
NC_000019.8:g.19190825T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252575.11:c.175T= MANE Select ENSP00000252575.4:p.Cys59=
ENST00000252575.10:c.175T= ENSP00000252575.4:p.Cys59=
NM_004386.2:c.175T= NP_004377.2:p.Cys59=
XM_005259747.1:c.175T= XP_005259804.1:p.Cys59=
NM_004386.3:c.175T= MANE Select NP_004377.2:p.Cys59=