Canonical Allele Identifier: CA357236388

Gene: AFP

Linked Data

• MyVariant Identifiers: chr4:g.74308015T>G (hg19) ; chr4:g.73442298T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442298T>G , CM000666.2:g.73442298T>G	GRCh38
NC_000004.11:g.74308015T>G , CM000666.1:g.74308015T>G	GRCh37
NC_000004.10:g.74526879T>G	NCBI36
NG_023028.1:g.11083T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.485T>G MANE Select	ENSP00000379138.2:p.Phe162Cys
ENST00000226359.2:c.485T>G	ENSP00000226359.2:p.Phe162Cys
ENST00000395792.6:c.485T>G	ENSP00000379138.2:p.Phe162Cys
NM_001134.2:c.485T>G	NP_001125.1:p.Phe162Cys
XM_011531704.1:c.482T>G	XP_011530006.1:p.Phe161Cys
NM_001354717.1:c.11T>G	NP_001341646.1:p.Phe4Cys
NM_001134.3:c.485T>G MANE Select	NP_001125.1:p.Phe162Cys
NM_001354717.2:c.11T>G	NP_001341646.2:p.Phe4Cys