Canonical Allele Identifier: CA2583147627
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897716_15897717del , CM000681.2:g.15897716_15897717del GRCh38
NC_000019.9:g.16008526_16008527del , CM000681.1:g.16008526_16008527del GRCh37
NC_000019.8:g.15869526_15869527del NCBI36
NG_007971.2:g.5360_5361del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-103_-1-102del MANE Select ENSP00000221700.3:n.-1-103_-1-102del
ENST00000011989.11:c.-1-103_-1-102del ENSP00000011989.8:n.-1-103_-1-102del
ENST00000221700.10:c.-1-103_-1-102del ENSP00000221700.3:n.-1-103_-1-102del
ENST00000392846.7:n.49+311_49+312del
ENST00000586927.2:c.-104_-103del ENSP00000465514.1:n.-104_-103del
ENST00000587671.2:c.-1-103_-1-102del ENSP00000467443.2:n.-1-103_-1-102del
ENST00000608168.1:n.53-103_53-102del
NM_001082.4:c.-1-103_-1-102del NP_001073.3:n.-1-103_-1-102del
NM_001082.5:c.-1-103_-1-102del MANE Select NP_001073.3:n.-1-103_-1-102del