Canonical Allele Identifier: CA1519891297

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208885A= , CM000666.2:g.186208885A=	GRCh38
NC_000004.11:g.187130039A= , CM000666.1:g.187130039A=	GRCh37
NC_000004.10:g.187367033A=	NCBI36
NG_007965.1:g.22366A=
NG_012095.2:g.4907A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1111A= MANE Select	ENSP00000368079.4:p.Thr371=
ENST00000378802.4:c.1111A=	ENSP00000368079.4:p.Thr371=
ENST00000502665.1:n.346A=
ENST00000507209.5:n.5809A=
ENST00000513354.5:n.201A=
NM_207352.3:c.1111A=	NP_997235.3:p.Thr371=
XM_005262935.2:c.1111A=	XP_005262992.1:p.Thr371=
XM_006714184.2:c.715A=	XP_006714247.1:p.Thr239=
XM_005262935.4:c.1111A=	XP_005262992.1:p.Thr371=
XM_017008037.1:c.715A=	XP_016863526.1:p.Thr239=
NM_207352.4:c.1111A= MANE Select	NP_997235.3:p.Thr371=