Canonical Allele Identifier: CA442638752

Gene: CYP4V2

Linked Data

• COSMIC: COSM4831203
• MyVariant Identifiers: chr4:g.187115763G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194609G>T , CM000666.2:g.186194609G>T	GRCh38
NC_000004.11:g.187115763G>T , CM000666.1:g.187115763G>T	GRCh37
NC_000004.10:g.187352757G>T	NCBI36
NG_007965.1:g.8090G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.324G>T MANE Select	ENSP00000368079.4:p.Val108=
ENST00000378802.4:c.324G>T	ENSP00000368079.4:p.Val108=
NM_207352.3:c.324G>T	NP_997235.3:p.Val108=
XM_005262935.2:c.324G>T	XP_005262992.1:p.Val108=
XM_006714184.2:c.14G>T	XP_006714247.1:p.Trp5Leu
XM_005262935.4:c.324G>T	XP_005262992.1:p.Val108=
XM_017008037.1:c.14G>T	XP_016863526.1:p.Trp5Leu
NM_207352.4:c.324G>T MANE Select	NP_997235.3:p.Val108=