Canonical Allele Identifier: CA417755861

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398486T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932814T>A , CM000663.2:g.46932814T>A	GRCh38
NC_000001.10:g.47398486T>A , CM000663.1:g.47398486T>A	GRCh37
NC_000001.9:g.47171073T>A	NCBI36
NG_007932.1:g.13671A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1311A>T MANE Select	ENSP00000311095.4:p.Ala437=
ENST00000310638.8:c.1311A>T	ENSP00000311095.4:p.Ala437=
ENST00000371904.8:c.1314A>T	ENSP00000360971.4:p.Ala438=
ENST00000371905.1:c.1311A>T	ENSP00000360972.1:p.Ala437=
ENST00000462347.5:c.1017A>T	ENSP00000477495.1:p.Ala339=
ENST00000465874.5:c.*109A>T	ENSP00000476368.1:n.*109A>T
ENST00000468629.5:c.*16A>T	ENSP00000476619.1:n.*16A>T
ENST00000474458.5:c.*16A>T	ENSP00000476988.1:n.*16A>T
ENST00000475477.5:c.*105A>T	ENSP00000476854.1:n.*105A>T
NM_000778.3:c.1311A>T	NP_000769.2:p.Ala437=
XM_005270539.1:c.1017A>T	XP_005270596.1:p.Ala339=
XM_011540826.1:c.1329A>T	XP_011539128.1:p.Ala443=
XM_011540827.1:c.1035A>T	XP_011539129.1:p.Ala345=
XM_011540828.1:c.1017A>T	XP_011539130.1:p.Ala339=
XR_246241.1:n.1215A>T
XR_246242.1:n.1199A>T
NM_001319155.1:c.1215A>T	NP_001306084.1:p.Ala405=
NM_001363587.1:c.1017A>T	NP_001350516.1:p.Ala339=
NR_134988.1:n.1016A>T
NR_134989.1:n.1207A>T
NR_134990.1:n.1201A>T
NR_134991.1:n.1188A>T
NR_134992.1:n.817A>T
NR_134993.1:n.951A>T
NR_134994.1:n.1223A>T
XM_017000465.1:c.999A>T	XP_016855954.1:p.Ala333=
XR_001737005.1:n.1289A>T
NM_000778.4:c.1311A>T MANE Select	NP_000769.2:p.Ala437=
NM_001319155.2:c.1215A>T	NP_001306084.1:p.Ala405=
NM_001363587.2:c.1017A>T	NP_001350516.1:p.Ala339=
NR_134988.2:n.1008A>T
NR_134989.2:n.1199A>T
NR_134990.2:n.1193A>T
NR_134991.2:n.1180A>T
NR_134992.2:n.809A>T
NR_134993.2:n.943A>T
NR_134994.2:n.1215A>T