Canonical Allele Identifier: CA357236650

Gene: AFP

Linked Data

• MyVariant Identifiers: chr4:g.74308075C>A (hg19) ; chr4:g.73442358C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442358C>A , CM000666.2:g.73442358C>A	GRCh38
NC_000004.11:g.74308075C>A , CM000666.1:g.74308075C>A	GRCh37
NC_000004.10:g.74526939C>A	NCBI36
NG_023028.1:g.11143C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.545C>A MANE Select	ENSP00000379138.2:p.Ala182Asp
ENST00000226359.2:c.545C>A	ENSP00000226359.2:p.Ala182Asp
ENST00000395792.6:c.545C>A	ENSP00000379138.2:p.Ala182Asp
NM_001134.2:c.545C>A	NP_001125.1:p.Ala182Asp
XM_011531704.1:c.542C>A	XP_011530006.1:p.Ala181Asp
NM_001354717.1:c.71C>A	NP_001341646.1:p.Ala24Asp
NM_001134.3:c.545C>A MANE Select	NP_001125.1:p.Ala182Asp
NM_001354717.2:c.71C>A	NP_001341646.2:p.Ala24Asp