Canonical Allele Identifier: CA417755880

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398492A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932820A>G , CM000663.2:g.46932820A>G	GRCh38
NC_000001.10:g.47398492A>G , CM000663.1:g.47398492A>G	GRCh37
NC_000001.9:g.47171079A>G	NCBI36
NG_007932.1:g.13665T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1305T>C MANE Select	ENSP00000311095.4:p.Arg435=
ENST00000310638.8:c.1305T>C	ENSP00000311095.4:p.Arg435=
ENST00000371904.8:c.1308T>C	ENSP00000360971.4:p.Arg436=
ENST00000371905.1:c.1305T>C	ENSP00000360972.1:p.Arg435=
ENST00000462347.5:c.1011T>C	ENSP00000477495.1:p.Arg337=
ENST00000465874.5:c.*103T>C	ENSP00000476368.1:n.*103T>C
ENST00000468629.5:c.*10T>C	ENSP00000476619.1:n.*10T>C
ENST00000474458.5:c.*10T>C	ENSP00000476988.1:n.*10T>C
ENST00000475477.5:c.*99T>C	ENSP00000476854.1:n.*99T>C
NM_000778.3:c.1305T>C	NP_000769.2:p.Arg435=
XM_005270539.1:c.1011T>C	XP_005270596.1:p.Arg337=
XM_011540826.1:c.1323T>C	XP_011539128.1:p.Arg441=
XM_011540827.1:c.1029T>C	XP_011539129.1:p.Arg343=
XM_011540828.1:c.1011T>C	XP_011539130.1:p.Arg337=
XR_246241.1:n.1209T>C
XR_246242.1:n.1193T>C
NM_001319155.1:c.1209T>C	NP_001306084.1:p.Arg403=
NM_001363587.1:c.1011T>C	NP_001350516.1:p.Arg337=
NR_134988.1:n.1010T>C
NR_134989.1:n.1201T>C
NR_134990.1:n.1195T>C
NR_134991.1:n.1182T>C
NR_134992.1:n.811T>C
NR_134993.1:n.945T>C
NR_134994.1:n.1217T>C
XM_017000465.1:c.993T>C	XP_016855954.1:p.Arg331=
XR_001737005.1:n.1283T>C
NM_000778.4:c.1305T>C MANE Select	NP_000769.2:p.Arg435=
NM_001319155.2:c.1209T>C	NP_001306084.1:p.Arg403=
NM_001363587.2:c.1011T>C	NP_001350516.1:p.Arg337=
NR_134988.2:n.1002T>C
NR_134989.2:n.1193T>C
NR_134990.2:n.1187T>C
NR_134991.2:n.1174T>C
NR_134992.2:n.803T>C
NR_134993.2:n.937T>C
NR_134994.2:n.1209T>C