Canonical Allele Identifier: CA2583145353
Gene: CYP4F2 HGNC NCBI

Linked Data

gnomAD v4: 19-15879214-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879217del , CM000681.2:g.15879217del GRCh38
NC_000019.9:g.15990027del , CM000681.1:g.15990027del GRCh37
NC_000019.8:g.15851027del NCBI36
NG_007971.2:g.23860del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1397+131del MANE Select ENSP00000221700.3:n.1397+131del
ENST00000011989.11:c.1397+131del ENSP00000011989.8:n.1397+131del
ENST00000221700.10:c.1397+131del ENSP00000221700.3:n.1397+131del
ENST00000392846.7:n.1340+131del
ENST00000589654.2:c.185+131del
NM_001082.4:c.1397+131del NP_001073.3:n.1397+131del
NM_001082.5:c.1397+131del MANE Select NP_001073.3:n.1397+131del
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Search 100 bp 3'