Canonical Allele Identifier: CA1519914816

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194410_186194411delinsAT , CM000666.2:g.186194410_186194411delinsAT	GRCh38
NC_000004.11:g.187115564_187115565delinsAT , CM000666.1:g.187115564_187115565delinsAT	GRCh37
NC_000004.10:g.187352558_187352559delinsAT	NCBI36
NG_007965.1:g.7891_7892delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.215-90_215-89delinsAT MANE Select	ENSP00000368079.4:n.215-90_215-89delinsAT...
ENST00000378802.4:c.215-90_215-89delinsAT	ENSP00000368079.4:n.215-90_215-89delinsAT...
NM_207352.3:c.215-90_215-89delinsAT	NP_997235.3:n.215-90_215-89delinsAT
XM_005262935.2:c.215-90_215-89delinsAT	XP_005262992.1:n.215-90_215-89delinsAT
XM_005262935.4:c.215-90_215-89delinsAT	XP_005262992.1:n.215-90_215-89delinsAT
XM_017008037.1:c.-96-90_-96-89delinsAT	XP_016863526.1:n.-96-90_-96-89delinsAT
NM_207352.4:c.215-90_215-89delinsAT MANE Select	NP_997235.3:n.215-90_215-89delinsAT