Canonical Allele Identifier: CA2325105404

Gene: CYP4F2

Linked Data

• dbSNP Id: rs2089452616

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897157_15897158insT , CM000681.2:g.15897157_15897158insT	GRCh38
NC_000019.9:g.16007967_16007968insT , CM000681.1:g.16007967_16007968insT	GRCh37
NC_000019.8:g.15868967_15868968insT	NCBI36
NG_007971.2:g.5917_5918insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+256_198+257insA MANE Select	ENSP00000221700.3:n.198+256_198+257insA
ENST00000011989.11:c.198+256_198+257insA	ENSP00000011989.8:n.198+256_198+257insA
ENST00000221700.10:c.198+256_198+257insA	ENSP00000221700.3:n.198+256_198+257insA
ENST00000392846.7:n.49+868_49+869insA
ENST00000586927.2:c.198+256_198+257insA	ENSP00000465514.1:n.198+256_198+257insA
ENST00000587671.2:c.198+256_198+257insA	ENSP00000467443.2:n.198+256_198+257insA
ENST00000608168.1:n.251+256_251+257insA
NM_001082.4:c.198+256_198+257insA	NP_001073.3:n.198+256_198+257insA
NM_001082.5:c.198+256_198+257insA MANE Select	NP_001073.3:n.198+256_198+257insA