Canonical Allele Identifier: CA340223208

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1171226914
• MyVariant Identifiers: chr1:g.47398488C>T (hg19) ; chr1:g.46932816C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932816C>T , CM000663.2:g.46932816C>T	GRCh38
NC_000001.10:g.47398488C>T , CM000663.1:g.47398488C>T	GRCh37
NC_000001.9:g.47171075C>T	NCBI36
NG_007932.1:g.13669G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1309G>A MANE Select	ENSP00000311095.4:p.Ala437Thr
ENST00000310638.8:c.1309G>A	ENSP00000311095.4:p.Ala437Thr
ENST00000371904.8:c.1312G>A	ENSP00000360971.4:p.Ala438Thr
ENST00000371905.1:c.1309G>A	ENSP00000360972.1:p.Ala437Thr
ENST00000462347.5:c.1015G>A	ENSP00000477495.1:p.Ala339Thr
ENST00000465874.5:c.*107G>A	ENSP00000476368.1:n.*107G>A
ENST00000468629.5:c.*14G>A	ENSP00000476619.1:n.*14G>A
ENST00000474458.5:c.*14G>A	ENSP00000476988.1:n.*14G>A
ENST00000475477.5:c.*103G>A	ENSP00000476854.1:n.*103G>A
NM_000778.3:c.1309G>A	NP_000769.2:p.Ala437Thr
XM_005270539.1:c.1015G>A	XP_005270596.1:p.Ala339Thr
XM_011540826.1:c.1327G>A	XP_011539128.1:p.Ala443Thr
XM_011540827.1:c.1033G>A	XP_011539129.1:p.Ala345Thr
XM_011540828.1:c.1015G>A	XP_011539130.1:p.Ala339Thr
XR_246241.1:n.1213G>A
XR_246242.1:n.1197G>A
NM_001319155.1:c.1213G>A	NP_001306084.1:p.Ala405Thr
NM_001363587.1:c.1015G>A	NP_001350516.1:p.Ala339Thr
NR_134988.1:n.1014G>A
NR_134989.1:n.1205G>A
NR_134990.1:n.1199G>A
NR_134991.1:n.1186G>A
NR_134992.1:n.815G>A
NR_134993.1:n.949G>A
NR_134994.1:n.1221G>A
XM_017000465.1:c.997G>A	XP_016855954.1:p.Ala333Thr
XR_001737005.1:n.1287G>A
NM_000778.4:c.1309G>A MANE Select	NP_000769.2:p.Ala437Thr
NM_001319155.2:c.1213G>A	NP_001306084.1:p.Ala405Thr
NM_001363587.2:c.1015G>A	NP_001350516.1:p.Ala339Thr
NR_134988.2:n.1006G>A
NR_134989.2:n.1197G>A
NR_134990.2:n.1191G>A
NR_134991.2:n.1178G>A
NR_134992.2:n.807G>A
NR_134993.2:n.941G>A
NR_134994.2:n.1213G>A