Canonical Allele Identifier: CA357236457

Gene: AFP

Linked Data

• MyVariant Identifiers: chr4:g.74308029G>T (hg19) ; chr4:g.73442312G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442312G>T , CM000666.2:g.73442312G>T	GRCh38
NC_000004.11:g.74308029G>T , CM000666.1:g.74308029G>T	GRCh37
NC_000004.10:g.74526893G>T	NCBI36
NG_023028.1:g.11097G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.499G>T MANE Select	ENSP00000379138.2:p.Ala167Ser
ENST00000226359.2:c.499G>T	ENSP00000226359.2:p.Ala167Ser
ENST00000395792.6:c.499G>T	ENSP00000379138.2:p.Ala167Ser
NM_001134.2:c.499G>T	NP_001125.1:p.Ala167Ser
XM_011531704.1:c.496G>T	XP_011530006.1:p.Ala166Ser
NM_001354717.1:c.25G>T	NP_001341646.1:p.Ala9Ser
NM_001134.3:c.499G>T MANE Select	NP_001125.1:p.Ala167Ser
NM_001354717.2:c.25G>T	NP_001341646.2:p.Ala9Ser