Canonical Allele Identifier: CA357236670

Gene: AFP

Linked Data

• MyVariant Identifiers: chr4:g.74308081G>C (hg19) ; chr4:g.73442364G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73442364G>C , CM000666.2:g.73442364G>C	GRCh38
NC_000004.11:g.74308081G>C , CM000666.1:g.74308081G>C	GRCh37
NC_000004.10:g.74526945G>C	NCBI36
NG_023028.1:g.11149G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.551G>C MANE Select	ENSP00000379138.2:p.Arg184Pro
ENST00000226359.2:c.551G>C	ENSP00000226359.2:p.Arg184Pro
ENST00000395792.6:c.551G>C	ENSP00000379138.2:p.Arg184Pro
NM_001134.2:c.551G>C	NP_001125.1:p.Arg184Pro
XM_011531704.1:c.548G>C	XP_011530006.1:p.Arg183Pro
NM_001354717.1:c.77G>C	NP_001341646.1:p.Arg26Pro
NM_001134.3:c.551G>C MANE Select	NP_001125.1:p.Arg184Pro
NM_001354717.2:c.77G>C	NP_001341646.2:p.Arg26Pro