Canonical Allele Identifier: CA2764868361

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199136_186199137insA , CM000666.2:g.186199136_186199137insA	GRCh38
NC_000004.11:g.187120290_187120291insA , CM000666.1:g.187120290_187120291insA	GRCh37
NC_000004.10:g.187357284_187357285insA	NCBI36
NG_007965.1:g.12617_12618insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.801+53_801+54insA MANE Select	ENSP00000368079.4:n.801+53_801+54insA
ENST00000378802.4:c.801+53_801+54insA	ENSP00000368079.4:n.801+53_801+54insA
ENST00000507209.5:n.1642+53_1642+54insA
NM_207352.3:c.801+53_801+54insA	NP_997235.3:n.801+53_801+54insA
XM_005262935.2:c.801+53_801+54insA	XP_005262992.1:n.801+53_801+54insA
XM_006714184.2:c.405+53_405+54insA	XP_006714247.1:n.405+53_405+54insA
XM_005262935.4:c.801+53_801+54insA	XP_005262992.1:n.801+53_801+54insA
XM_017008037.1:c.405+53_405+54insA	XP_016863526.1:n.405+53_405+54insA
NM_207352.4:c.801+53_801+54insA MANE Select	NP_997235.3:n.801+53_801+54insA