Canonical Allele Identifier: CA2764868171

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205414_186205415insA , CM000666.2:g.186205414_186205415insA	GRCh38
NC_000004.11:g.187126568_187126569insA , CM000666.1:g.187126568_187126569insA	GRCh37
NC_000004.10:g.187363562_187363563insA	NCBI36
NG_007965.1:g.18895_18896insA
NG_012095.2:g.1436_1437insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+112_1090+113insA MANE Select	ENSP00000368079.4:n.1090+112_1090+113insA
ENST00000378802.4:c.1090+112_1090+113insA	ENSP00000368079.4:n.1090+112_1090+113insA
ENST00000502665.1:n.325+112_325+113insA
ENST00000507209.5:n.5788+112_5788+113insA
ENST00000513354.5:n.180+112_180+113insA
NM_207352.3:c.1090+112_1090+113insA	NP_997235.3:n.1090+112_1090+113insA
XM_005262935.2:c.1090+112_1090+113insA	XP_005262992.1:n.1090+112_1090+113insA
XM_006714184.2:c.694+112_694+113insA	XP_006714247.1:n.694+112_694+113insA
XM_005262935.4:c.1090+112_1090+113insA	XP_005262992.1:n.1090+112_1090+113insA
XM_017008037.1:c.694+112_694+113insA	XP_016863526.1:n.694+112_694+113insA
NM_207352.4:c.1090+112_1090+113insA MANE Select	NP_997235.3:n.1090+112_1090+113insA