Canonical Allele Identifier: CA305910108
Gene: CYP4F2 HGNC NCBI

Linked Data

dbSNP Id: rs755712778
MyVariant Identifiers: chr19:g.16008513_16008538del (hg19) chr19:g.15897703_15897728del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897703_15897728del , CM000681.2:g.15897703_15897728del GRCh38
NC_000019.9:g.16008513_16008538del , CM000681.1:g.16008513_16008538del GRCh37
NC_000019.8:g.15869513_15869538del NCBI36
NG_007971.2:g.5347_5372del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-116_-1-91del MANE Select ENSP00000221700.3:n.-1-116_-1-91del
ENST00000011989.11:c.-1-116_-1-91del ENSP00000011989.8:n.-1-116_-1-91del
ENST00000221700.10:c.-1-116_-1-91del ENSP00000221700.3:n.-1-116_-1-91del
ENST00000392846.7:n.49+298_49+323del
ENST00000586927.2:c.-117_-92del ENSP00000465514.1:n.-117_-92del
ENST00000587671.2:c.-1-116_-1-91del ENSP00000467443.2:n.-1-116_-1-91del
ENST00000608168.1:n.53-116_53-91del
NM_001082.4:c.-1-116_-1-91del NP_001073.3:n.-1-116_-1-91del
NM_001082.5:c.-1-116_-1-91del MANE Select NP_001073.3:n.-1-116_-1-91del
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