Canonical Allele Identifier: CA404906881

Gene: NCAN

Linked Data

• MyVariant Identifiers: chr19:g.19329834A>G (hg19) ; chr19:g.19219025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19219025A>G , CM000681.2:g.19219025A>G	GRCh38
NC_000019.9:g.19329834A>G , CM000681.1:g.19329834A>G	GRCh37
NC_000019.8:g.19190834A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000252575.11:c.184A>G MANE Select	ENSP00000252575.4:p.Thr62Ala
ENST00000252575.10:c.184A>G	ENSP00000252575.4:p.Thr62Ala
NM_004386.2:c.184A>G	NP_004377.2:p.Thr62Ala
XM_005259747.1:c.184A>G	XP_005259804.1:p.Thr62Ala
NM_004386.3:c.184A>G MANE Select	NP_004377.2:p.Thr62Ala