Canonical Allele Identifier: CA2583145409
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879273dup , CM000681.2:g.15879273dup GRCh38
NC_000019.9:g.15990083dup , CM000681.1:g.15990083dup GRCh37
NC_000019.8:g.15851083dup NCBI36
NG_007971.2:g.23806dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+77dup MANE Select ENSP00000221700.3:n.1397+77dup
ENST00000011989.11:c.1397+77dup ENSP00000011989.8:n.1397+77dup
ENST00000221700.10:c.1397+77dup ENSP00000221700.3:n.1397+77dup
ENST00000392846.7:n.1340+77dup
ENST00000589654.2:c.185+77dup
NM_001082.4:c.1397+77dup NP_001073.3:n.1397+77dup
NM_001082.5:c.1397+77dup MANE Select NP_001073.3:n.1397+77dup