Canonical Allele Identifier: CA2708144496

Gene: CYP4V2

Linked Data

• dbSNP Id: rs2126600423

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208821_186208848del , CM000666.2:g.186208821_186208848del	GRCh38
NC_000004.11:g.187129975_187130002del , CM000666.1:g.187129975_187130002del	GRCh37
NC_000004.10:g.187366969_187366996del	NCBI36
NG_007965.1:g.22302_22329del
NG_012095.2:g.4843_4870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-44_1091-17del MANE Select	ENSP00000368079.4:n.1091-44_1091-17del
ENST00000378802.4:c.1091-44_1091-17del	ENSP00000368079.4:n.1091-44_1091-17del
ENST00000502665.1:n.326-44_326-17del
ENST00000507209.5:n.5789-44_5789-17del
ENST00000513354.5:n.181-44_181-17del
NM_207352.3:c.1091-44_1091-17del	NP_997235.3:n.1091-44_1091-17del
XM_005262935.2:c.1091-44_1091-17del	XP_005262992.1:n.1091-44_1091-17del
XM_006714184.2:c.695-44_695-17del	XP_006714247.1:n.695-44_695-17del
XM_005262935.4:c.1091-44_1091-17del	XP_005262992.1:n.1091-44_1091-17del
XM_017008037.1:c.695-44_695-17del	XP_016863526.1:n.695-44_695-17del
NM_207352.4:c.1091-44_1091-17del MANE Select	NP_997235.3:n.1091-44_1091-17del