Canonical Allele Identifier: CA417755725
Gene: CYP4A11 HGNC NCBI

Linked Data

gnomAD v4: 1-46932763-T-C
MyVariant Identifiers: chr1:g.47398435T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932763T>C , CM000663.2:g.46932763T>C GRCh38
NC_000001.10:g.47398435T>C , CM000663.1:g.47398435T>C GRCh37
NC_000001.9:g.47171022T>C NCBI36
NG_007932.1:g.13722A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1362A>G MANE Select ENSP00000311095.4:p.Ser454=
ENST00000310638.8:c.1362A>G ENSP00000311095.4:p.Ser454=
ENST00000371904.8:c.1365A>G ENSP00000360971.4:p.Ser455=
ENST00000371905.1:c.1362A>G ENSP00000360972.1:p.Ser454=
ENST00000462347.5:c.1068A>G ENSP00000477495.1:p.Ser356=
ENST00000465874.5:c.*160A>G ENSP00000476368.1:n.*160A>G
ENST00000468629.5:c.*67A>G ENSP00000476619.1:n.*67A>G
ENST00000474458.5:c.*67A>G ENSP00000476988.1:n.*67A>G
ENST00000475477.5:c.*156A>G ENSP00000476854.1:n.*156A>G
NM_000778.3:c.1362A>G NP_000769.2:p.Ser454=
XM_005270539.1:c.1068A>G XP_005270596.1:p.Ser356=
XM_011540826.1:c.1380A>G XP_011539128.1:p.Ser460=
XM_011540827.1:c.1086A>G XP_011539129.1:p.Ser362=
XM_011540828.1:c.1068A>G XP_011539130.1:p.Ser356=
XR_246241.1:n.1266A>G
XR_246242.1:n.1250A>G
NM_001319155.1:c.1266A>G NP_001306084.1:p.Ser422=
NM_001363587.1:c.1068A>G NP_001350516.1:p.Ser356=
NR_134988.1:n.1067A>G
NR_134989.1:n.1258A>G
NR_134990.1:n.1252A>G
NR_134991.1:n.1239A>G
NR_134992.1:n.868A>G
NR_134993.1:n.1002A>G
NR_134994.1:n.1274A>G
XM_017000465.1:c.1050A>G XP_016855954.1:p.Ser350=
XR_001737005.1:n.1340A>G
NM_000778.4:c.1362A>G MANE Select NP_000769.2:p.Ser454=
NM_001319155.2:c.1266A>G NP_001306084.1:p.Ser422=
NM_001363587.2:c.1068A>G NP_001350516.1:p.Ser356=
NR_134988.2:n.1059A>G
NR_134989.2:n.1250A>G
NR_134990.2:n.1244A>G
NR_134991.2:n.1231A>G
NR_134992.2:n.860A>G
NR_134993.2:n.994A>G
NR_134994.2:n.1266A>G