Canonical Allele Identifier: CA2325096797

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879145_15879146delinsGA , CM000681.2:g.15879145_15879146delinsGA	GRCh38
NC_000019.9:g.15989955_15989956delinsGA , CM000681.1:g.15989955_15989956delinsGA	GRCh37
NC_000019.8:g.15850955_15850956delinsGA	NCBI36
NG_007971.2:g.23929_23930delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+200_1397+201delinsTC MANE Select	ENSP00000221700.3:n.1397+200_1397+201delinsTC
ENST00000011989.11:c.1397+200_1397+201delinsTC	ENSP00000011989.8:n.1397+200_1397+201delinsTC
ENST00000221700.10:c.1397+200_1397+201delinsTC	ENSP00000221700.3:n.1397+200_1397+201delinsTC
ENST00000392846.7:n.1340+200_1340+201delinsTC
ENST00000589654.2:c.185+200_185+201delinsTC
NM_001082.4:c.1397+200_1397+201delinsTC	NP_001073.3:n.1397+200_1397+201delinsTC
NM_001082.5:c.1397+200_1397+201delinsTC MANE Select	NP_001073.3:n.1397+200_1397+201delinsTC