Canonical Allele Identifier: CA2764867682

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204661_186204662insA , CM000666.2:g.186204661_186204662insA	GRCh38
NC_000004.11:g.187125815_187125816insA , CM000666.1:g.187125815_187125816insA	GRCh37
NC_000004.10:g.187362809_187362810insA	NCBI36
NG_007965.1:g.18142_18143insA
NG_012095.2:g.683_684insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-539_988-538insA MANE Select	ENSP00000368079.4:n.988-539_988-538insA
ENST00000378802.4:c.988-539_988-538insA	ENSP00000368079.4:n.988-539_988-538insA
ENST00000507209.5:n.5147_5148insA
ENST00000513354.5:n.77+204_77+205insA
NM_207352.3:c.988-539_988-538insA	NP_997235.3:n.988-539_988-538insA
XM_005262935.2:c.988-539_988-538insA	XP_005262992.1:n.988-539_988-538insA
XM_006714184.2:c.592-539_592-538insA	XP_006714247.1:n.592-539_592-538insA
XM_005262935.4:c.988-539_988-538insA	XP_005262992.1:n.988-539_988-538insA
XM_017008037.1:c.592-539_592-538insA	XP_016863526.1:n.592-539_592-538insA
NM_207352.4:c.988-539_988-538insA MANE Select	NP_997235.3:n.988-539_988-538insA