Canonical Allele Identifier: CA1468189729

Gene: AFP

Linked Data

• dbSNP Id: rs1720146087

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73455915_73455920del , CM000666.2:g.73455915_73455920del	GRCh38
NC_000004.11:g.74321632_74321637del , CM000666.1:g.74321632_74321637del	GRCh37
NC_000004.10:g.74540496_74540501del	NCBI36
NG_023028.1:g.24700_24705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.*295_*300del MANE Select	ENSP00000379138.2:n.*295_*300del
ENST00000395792.6:c.*295_*300del	ENSP00000379138.2:n.*295_*300del
NM_001134.3:c.*295_*300del MANE Select	NP_001125.1:n.*295_*300del
NM_001354717.2:c.*295_*300del	NP_001341646.2:n.*295_*300del