Canonical Allele Identifier: CA2708144403

Gene: CYP4V2

Linked Data

• dbSNP Id: rs2126600216

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208687_186208689del , CM000666.2:g.186208687_186208689del	GRCh38
NC_000004.11:g.187129841_187129843del , CM000666.1:g.187129841_187129843del	GRCh37
NC_000004.10:g.187366835_187366837del	NCBI36
NG_007965.1:g.22168_22170del
NG_012095.2:g.4709_4711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-178_1091-176del MANE Select	ENSP00000368079.4:n.1091-178_1091-176del
ENST00000378802.4:c.1091-178_1091-176del	ENSP00000368079.4:n.1091-178_1091-176del
ENST00000502665.1:n.326-178_326-176del
ENST00000507209.5:n.5789-178_5789-176del
ENST00000513354.5:n.181-178_181-176del
NM_207352.3:c.1091-178_1091-176del	NP_997235.3:n.1091-178_1091-176del
XM_005262935.2:c.1091-178_1091-176del	XP_005262992.1:n.1091-178_1091-176del
XM_006714184.2:c.695-178_695-176del	XP_006714247.1:n.695-178_695-176del
XM_005262935.4:c.1091-178_1091-176del	XP_005262992.1:n.1091-178_1091-176del
XM_017008037.1:c.695-178_695-176del	XP_016863526.1:n.695-178_695-176del
NM_207352.4:c.1091-178_1091-176del MANE Select	NP_997235.3:n.1091-178_1091-176del