Canonical Allele Identifier: CA2764867624

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204625_186204626insAG , CM000666.2:g.186204625_186204626insAG	GRCh38
NC_000004.11:g.187125779_187125780insAG , CM000666.1:g.187125779_187125780insAG	GRCh37
NC_000004.10:g.187362773_187362774insAG	NCBI36
NG_007965.1:g.18106_18107insAG
NG_012095.2:g.647_648insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-575_988-574insAG MANE Select	ENSP00000368079.4:n.988-575_988-574insAG
ENST00000378802.4:c.988-575_988-574insAG	ENSP00000368079.4:n.988-575_988-574insAG
ENST00000507209.5:n.5111_5112insAG
ENST00000513354.5:n.77+168_77+169insAG
NM_207352.3:c.988-575_988-574insAG	NP_997235.3:n.988-575_988-574insAG
XM_005262935.2:c.988-575_988-574insAG	XP_005262992.1:n.988-575_988-574insAG
XM_006714184.2:c.592-575_592-574insAG	XP_006714247.1:n.592-575_592-574insAG
XM_005262935.4:c.988-575_988-574insAG	XP_005262992.1:n.988-575_988-574insAG
XM_017008037.1:c.592-575_592-574insAG	XP_016863526.1:n.592-575_592-574insAG
NM_207352.4:c.988-575_988-574insAG MANE Select	NP_997235.3:n.988-575_988-574insAG