Canonical Allele Identifier: CA1064127023

Gene: AFP

Linked Data

• dbSNP Id: rs1720148914
• gnomAD v3: 4-73456008-C-CATTTAAT
• gnomAD v4: 4-73456008-C-CATTTAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73456009_73456010insTTTAATA , CM000666.2:g.73456009_73456010insTTTAATA	GRCh38
NC_000004.11:g.74321726_74321727insTTTAATA , CM000666.1:g.74321726_74321727insTTTAATA	GRCh37
NC_000004.10:g.74540590_74540591insTTTAATA	NCBI36
NG_023028.1:g.24794_24795insTTTAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395792.7:c.*389_*390insTTTAATA MANE Select	ENSP00000379138.2:n.*389_*390insTTTAATA
ENST00000395792.6:c.*389_*390insTTTAATA	ENSP00000379138.2:n.*389_*390insTTTAATA
NM_001134.3:c.*389_*390insTTTAATA MANE Select	NP_001125.1:n.*389_*390insTTTAATA
NM_001354717.2:c.*389_*390insTTTAATA	NP_001341646.2:n.*389_*390insTTTAATA