Canonical Allele Identifier: CA2326737228
Gene: NCAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19219026C= , CM000681.2:g.19219026C= GRCh38
NC_000019.9:g.19329835C= , CM000681.1:g.19329835C= GRCh37
NC_000019.8:g.19190835C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252575.11:c.185C= MANE Select ENSP00000252575.4:p.Thr62=
ENST00000252575.10:c.185C= ENSP00000252575.4:p.Thr62=
NM_004386.2:c.185C= NP_004377.2:p.Thr62=
XM_005259747.1:c.185C= XP_005259804.1:p.Thr62=
NM_004386.3:c.185C= MANE Select NP_004377.2:p.Thr62=