Canonical Allele Identifier: CA358950252

Gene: CYP4V2

Linked Data

• COSMIC: COSM3131108
• MyVariant Identifiers: chr4:g.187130114C>T (hg19) ; chr4:g.186208960C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208960C>T , CM000666.2:g.186208960C>T	GRCh38
NC_000004.11:g.187130114C>T , CM000666.1:g.187130114C>T	GRCh37
NC_000004.10:g.187367108C>T	NCBI36
NG_007965.1:g.22441C>T
NG_012095.2:g.4982C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1186C>T MANE Select	ENSP00000368079.4:p.Pro396Ser
ENST00000378802.4:c.1186C>T	ENSP00000368079.4:p.Pro396Ser
ENST00000502665.1:n.421C>T
ENST00000507209.5:n.5884C>T
ENST00000513354.5:n.276C>T
NM_207352.3:c.1186C>T	NP_997235.3:p.Pro396Ser
XM_005262935.2:c.1186C>T	XP_005262992.1:p.Pro396Ser
XM_006714184.2:c.790C>T	XP_006714247.1:p.Pro264Ser
XM_005262935.4:c.1186C>T	XP_005262992.1:p.Pro396Ser
XM_017008037.1:c.790C>T	XP_016863526.1:p.Pro264Ser
NM_207352.4:c.1186C>T MANE Select	NP_997235.3:p.Pro396Ser