Canonical Allele Identifier: CA1519889048

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205280_186205281delinsTC , CM000666.2:g.186205280_186205281delinsTC	GRCh38
NC_000004.11:g.187126434_187126435delinsTC , CM000666.1:g.187126434_187126435delinsTC	GRCh37
NC_000004.10:g.187363428_187363429delinsTC	NCBI36
NG_007965.1:g.18761_18762delinsTC
NG_012095.2:g.1302_1303delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1068_1069delinsTC MANE Select	ENSP00000368079.4:p.Asp356=
ENST00000378802.4:c.1068_1069delinsTC	ENSP00000368079.4:p.Asp356=
ENST00000502665.1:n.303_304delinsTC
ENST00000507209.5:n.5766_5767delinsTC
ENST00000513354.5:n.158_159delinsTC
NM_207352.3:c.1068_1069delinsTC	NP_997235.3:p.Asp356=
XM_005262935.2:c.1068_1069delinsTC	XP_005262992.1:p.Asp356=
XM_006714184.2:c.672_673delinsTC	XP_006714247.1:p.Asp224=
XM_005262935.4:c.1068_1069delinsTC	XP_005262992.1:p.Asp356=
XM_017008037.1:c.672_673delinsTC	XP_016863526.1:p.Asp224=
NM_207352.4:c.1068_1069delinsTC MANE Select	NP_997235.3:p.Asp356=