Canonical Allele Identifier: CA2764867723

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204686_186204687insA , CM000666.2:g.186204686_186204687insA	GRCh38
NC_000004.11:g.187125840_187125841insA , CM000666.1:g.187125840_187125841insA	GRCh37
NC_000004.10:g.187362834_187362835insA	NCBI36
NG_007965.1:g.18167_18168insA
NG_012095.2:g.708_709insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-514_988-513insA MANE Select	ENSP00000368079.4:n.988-514_988-513insA
ENST00000378802.4:c.988-514_988-513insA	ENSP00000368079.4:n.988-514_988-513insA
ENST00000507209.5:n.5172_5173insA
ENST00000513354.5:n.77+229_77+230insA
NM_207352.3:c.988-514_988-513insA	NP_997235.3:n.988-514_988-513insA
XM_005262935.2:c.988-514_988-513insA	XP_005262992.1:n.988-514_988-513insA
XM_006714184.2:c.592-514_592-513insA	XP_006714247.1:n.592-514_592-513insA
XM_005262935.4:c.988-514_988-513insA	XP_005262992.1:n.988-514_988-513insA
XM_017008037.1:c.592-514_592-513insA	XP_016863526.1:n.592-514_592-513insA
NM_207352.4:c.988-514_988-513insA MANE Select	NP_997235.3:n.988-514_988-513insA