Canonical Allele Identifier: CA2764867860

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204775_186204776insACA , CM000666.2:g.186204775_186204776insACA	GRCh38
NC_000004.11:g.187125929_187125930insACA , CM000666.1:g.187125929_187125930insACA	GRCh37
NC_000004.10:g.187362923_187362924insACA	NCBI36
NG_007965.1:g.18256_18257insACA
NG_012095.2:g.797_798insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-425_988-424insACA MANE Select	ENSP00000368079.4:n.988-425_988-424insACA
ENST00000378802.4:c.988-425_988-424insACA	ENSP00000368079.4:n.988-425_988-424insACA
ENST00000507209.5:n.5261_5262insACA
ENST00000513354.5:n.77+318_77+319insACA
NM_207352.3:c.988-425_988-424insACA	NP_997235.3:n.988-425_988-424insACA
XM_005262935.2:c.988-425_988-424insACA	XP_005262992.1:n.988-425_988-424insACA
XM_006714184.2:c.592-425_592-424insACA	XP_006714247.1:n.592-425_592-424insACA
XM_005262935.4:c.988-425_988-424insACA	XP_005262992.1:n.988-425_988-424insACA
XM_017008037.1:c.592-425_592-424insACA	XP_016863526.1:n.592-425_592-424insACA
NM_207352.4:c.988-425_988-424insACA MANE Select	NP_997235.3:n.988-425_988-424insACA