Canonical Allele Identifier: CA357236514

Gene: AFP

Linked Data

• MyVariant Identifiers: chr4:g.74308042C>T (hg19) ; chr4:g.73442325C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442325C>T , CM000666.2:g.73442325C>T	GRCh38
NC_000004.11:g.74308042C>T , CM000666.1:g.74308042C>T	GRCh37
NC_000004.10:g.74526906C>T	NCBI36
NG_023028.1:g.11110C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.512C>T MANE Select	ENSP00000379138.2:p.Pro171Leu
ENST00000226359.2:c.512C>T	ENSP00000226359.2:p.Pro171Leu
ENST00000395792.6:c.512C>T	ENSP00000379138.2:p.Pro171Leu
NM_001134.2:c.512C>T	NP_001125.1:p.Pro171Leu
XM_011531704.1:c.509C>T	XP_011530006.1:p.Pro170Leu
NM_001354717.1:c.38C>T	NP_001341646.1:p.Pro13Leu
NM_001134.3:c.512C>T MANE Select	NP_001125.1:p.Pro171Leu
NM_001354717.2:c.38C>T	NP_001341646.2:p.Pro13Leu