Canonical Allele Identifier: CA839263
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs778179068

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932737G>C , CM000663.2:g.46932737G>C GRCh38
NC_000001.10:g.47398409G>C , CM000663.1:g.47398409G>C GRCh37
NC_000001.9:g.47170996G>C NCBI36
NG_007932.1:g.13748C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+24C>G MANE Select ENSP00000311095.4:n.1364+24C>G
ENST00000310638.8:c.1364+24C>G ENSP00000311095.4:n.1364+24C>G
ENST00000371904.8:c.1367+24C>G ENSP00000360971.4:n.1367+24C>G
ENST00000371905.1:c.*20C>G ENSP00000360972.1:n.*20C>G
ENST00000462347.5:c.1070+24C>G ENSP00000477495.1:n.1070+24C>G
ENST00000465874.5:c.*186C>G ENSP00000476368.1:n.*186C>G
ENST00000468629.5:c.*69+24C>G ENSP00000476619.1:n.*69+24C>G
ENST00000474458.5:c.*69+24C>G ENSP00000476988.1:n.*69+24C>G
ENST00000475477.5:c.*158+24C>G ENSP00000476854.1:n.*158+24C>G
NM_000778.3:c.1364+24C>G NP_000769.2:n.1364+24C>G
XM_011540826.1:c.1382+24C>G XP_011539128.1:n.1382+24C>G
XM_011540827.1:c.1088+24C>G XP_011539129.1:n.1088+24C>G
XM_011540828.1:c.1070+24C>G XP_011539130.1:n.1070+24C>G
XR_246241.1:n.1268+24C>G
XR_246242.1:n.1252+24C>G
NM_001319155.1:c.1268+24C>G NP_001306084.1:n.1268+24C>G
NM_001363587.1:c.1070+24C>G NP_001350516.1:n.1070+24C>G
NR_134988.1:n.1069+24C>G
NR_134989.1:n.1260+24C>G
NR_134990.1:n.1254+24C>G
NR_134991.1:n.1241+24C>G
NR_134992.1:n.870+24C>G
NR_134993.1:n.1004+24C>G
NR_134994.1:n.1276+24C>G
XM_017000465.1:c.1052+24C>G XP_016855954.1:n.1052+24C>G
XR_001737005.1:n.1342+24C>G
NM_000778.4:c.1364+24C>G MANE Select NP_000769.2:n.1364+24C>G
NM_001319155.2:c.1268+24C>G NP_001306084.1:n.1268+24C>G
NM_001363587.2:c.1070+24C>G NP_001350516.1:n.1070+24C>G
NR_134988.2:n.1061+24C>G
NR_134989.2:n.1252+24C>G
NR_134990.2:n.1246+24C>G
NR_134991.2:n.1233+24C>G
NR_134992.2:n.862+24C>G
NR_134993.2:n.996+24C>G
NR_134994.2:n.1268+24C>G