Canonical Allele Identifier: CA2583147672
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897776_15897868del , CM000681.2:g.15897776_15897868del GRCh38
NC_000019.9:g.16008586_16008678del , CM000681.1:g.16008586_16008678del GRCh37
NC_000019.8:g.15869586_15869678del NCBI36
NG_007971.2:g.5226_5318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-2+177_-1-145del MANE Select ENSP00000221700.3:n.-2+177_-1-145del
ENST00000011989.11:c.-2+177_-1-145del ENSP00000011989.8:n.-2+177_-1-145del
ENST00000221700.10:c.-2+177_-1-145del ENSP00000221700.3:n.-2+177_-1-145del
ENST00000392846.7:n.49+177_49+269del
ENST00000587671.2:c.-2+177_-1-145del ENSP00000467443.2:n.-2+177_-1-145del
ENST00000608168.1:n.52+177_53-145del
NM_001082.4:c.-2+177_-1-145del NP_001073.3:n.-2+177_-1-145del
NM_001082.5:c.-2+177_-1-145del MANE Select NP_001073.3:n.-2+177_-1-145del