Canonical Allele Identifier: CA2695876754
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1681136167

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46933144A>C , CM000663.2:g.46933144A>C GRCh38
NC_000001.10:g.47398816A>C , CM000663.1:g.47398816A>C GRCh37
NC_000001.9:g.47171403A>C NCBI36
NG_007932.1:g.13341T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1223-97T>G MANE Select ENSP00000311095.4:n.1223-97T>G
ENST00000310638.8:c.1223-97T>G ENSP00000311095.4:n.1223-97T>G
ENST00000371904.8:c.1226-97T>G ENSP00000360971.4:n.1226-97T>G
ENST00000371905.1:c.1223-97T>G ENSP00000360972.1:n.1223-97T>G
ENST00000462347.5:c.929-97T>G ENSP00000477495.1:n.929-97T>G
ENST00000465874.5:c.*21-97T>G ENSP00000476368.1:n.*21-97T>G
ENST00000468629.5:c.1127-307T>G ENSP00000476619.1:n.1127-307T>G
ENST00000474458.5:c.743-307T>G ENSP00000476988.1:n.743-307T>G
ENST00000475477.5:c.*82-307T>G ENSP00000476854.1:n.*82-307T>G
NM_000778.3:c.1223-97T>G NP_000769.2:n.1223-97T>G
XM_005270539.1:c.929-97T>G XP_005270596.1:n.929-97T>G
XM_011540826.1:c.1241-97T>G XP_011539128.1:n.1241-97T>G
XM_011540827.1:c.947-97T>G XP_011539129.1:n.947-97T>G
XM_011540828.1:c.929-97T>G XP_011539130.1:n.929-97T>G
XR_246241.1:n.1127-97T>G
XR_246242.1:n.1111-97T>G
NM_001319155.1:c.1127-97T>G NP_001306084.1:n.1127-97T>G
NM_001363587.1:c.929-97T>G NP_001350516.1:n.929-97T>G
NR_134988.1:n.928-97T>G
NR_134989.1:n.1119-97T>G
NR_134990.1:n.1178-307T>G
NR_134991.1:n.1100-97T>G
NR_134992.1:n.794-307T>G
NR_134993.1:n.928-307T>G
NR_134994.1:n.1135-97T>G
XM_017000465.1:c.911-97T>G XP_016855954.1:n.911-97T>G
XR_001737005.1:n.1266-307T>G
NM_000778.4:c.1223-97T>G MANE Select NP_000769.2:n.1223-97T>G
NM_001319155.2:c.1127-97T>G NP_001306084.1:n.1127-97T>G
NM_001363587.2:c.929-97T>G NP_001350516.1:n.929-97T>G
NR_134988.2:n.920-97T>G
NR_134989.2:n.1111-97T>G
NR_134990.2:n.1170-307T>G
NR_134991.2:n.1092-97T>G
NR_134992.2:n.786-307T>G
NR_134993.2:n.920-307T>G
NR_134994.2:n.1127-97T>G