Canonical Allele Identifier: CA358949339

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187126400T>C (hg19) ; chr4:g.186205246T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205246T>C , CM000666.2:g.186205246T>C	GRCh38
NC_000004.11:g.187126400T>C , CM000666.1:g.187126400T>C	GRCh37
NC_000004.10:g.187363394T>C	NCBI36
NG_007965.1:g.18727T>C
NG_012095.2:g.1268T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1034T>C MANE Select	ENSP00000368079.4:p.Leu345Ser
ENST00000378802.4:c.1034T>C	ENSP00000368079.4:p.Leu345Ser
ENST00000502665.1:n.269T>C
ENST00000507209.5:n.5732T>C
ENST00000513354.5:n.124T>C
NM_207352.3:c.1034T>C	NP_997235.3:p.Leu345Ser
XM_005262935.2:c.1034T>C	XP_005262992.1:p.Leu345Ser
XM_006714184.2:c.638T>C	XP_006714247.1:p.Leu213Ser
XM_005262935.4:c.1034T>C	XP_005262992.1:p.Leu345Ser
XM_017008037.1:c.638T>C	XP_016863526.1:p.Leu213Ser
NM_207352.4:c.1034T>C MANE Select	NP_997235.3:p.Leu345Ser