Canonical Allele Identifier: CA358949187
Gene: CYP4V2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186205169del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205169del , CM000666.2:g.186205169del GRCh38
NC_000004.11:g.187126323del , CM000666.1:g.187126323del GRCh37
NC_000004.10:g.187363317del NCBI36
NG_007965.1:g.18650del
NG_012095.2:g.1191del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-31del MANE Select ENSP00000368079.4:n.988-31del
ENST00000378802.4:c.988-31del ENSP00000368079.4:n.988-31del
ENST00000502665.1:n.223-31del
ENST00000507209.5:n.5655del
ENST00000513354.5:n.78-31del
NM_207352.3:c.988-31del NP_997235.3:n.988-31del
XM_005262935.2:c.988-31del XP_005262992.1:n.988-31del
XM_006714184.2:c.592-31del XP_006714247.1:n.592-31del
XM_005262935.4:c.988-31del XP_005262992.1:n.988-31del
XM_017008037.1:c.592-31del XP_016863526.1:n.592-31del
NM_207352.4:c.988-31del MANE Select NP_997235.3:n.988-31del