Canonical Allele Identifier: CA2474390391
Gene: CYP4A11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932241_46932255delinsTGACTTGAAAGGTAG , CM000663.2:g.46932241_46932255delinsTGACTTGAAAGGTAG GRCh38
NC_000001.10:g.47397913_47397927delinsTGACTTGAAAGGTAG , CM000663.1:g.47397913_47397927delinsTGACTTGAAAGGTAG GRCh37
NC_000001.9:g.47170500_47170514delinsTGACTTGAAAGGTAG NCBI36
NG_007932.1:g.14230_14244delinsCTACCTTTCAAGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1364+506_1364+520delinsCTACCTTTCAAGTCA MANE Select ENSP00000311095.4:n.1364+506_1364+520delinsCTACCTTTCAAGTCA
ENST00000310638.8:c.1364+506_1364+520delinsCTACCTTTCAAGTCA ENSP00000311095.4:n.1364+506_1364+520delinsCTACCTTTCAAGTCA
ENST00000371904.8:c.1367+506_1367+520delinsCTACCTTTCAAGTCA ENSP00000360971.4:n.1367+506_1367+520delinsCTACCTTTCAAGTCA
ENST00000462347.5:c.1070+506_1070+520delinsCTACCTTTCAAGTCA ENSP00000477495.1:n.1070+506_1070+520delinsCTACCTTTCAAGTCA
ENST00000465874.5:c.*668_*682delinsCTACCTTTCAAGTCA ENSP00000476368.1:n.*668_*682delinsCTACCTTTCAAGTCA
ENST00000468629.5:c.*69+506_*69+520delinsCTACCTTTCAAGTCA ENSP00000476619.1:n.*69+506_*69+520delinsCTACCTTTCAAGTCA
ENST00000474458.5:c.*69+506_*69+520delinsCTACCTTTCAAGTCA ENSP00000476988.1:n.*69+506_*69+520delinsCTACCTTTCAAGTCA
ENST00000475477.5:c.*158+506_*158+520delinsCTACCTTTCAAGTCA ENSP00000476854.1:n.*158+506_*158+520delinsCTACCTTTCAAGTCA
NM_000778.3:c.1364+506_1364+520delinsCTACCTTTCAAGTCA NP_000769.2:n.1364+506_1364+520delinsCTACCTTTCAAGTCA
XM_011540826.1:c.1382+506_1382+520delinsCTACCTTTCAAGTCA XP_011539128.1:n.1382+506_1382+520delinsCTACCTTTCAAGTCA
XM_011540827.1:c.1088+506_1088+520delinsCTACCTTTCAAGTCA XP_011539129.1:n.1088+506_1088+520delinsCTACCTTTCAAGTCA
XM_011540828.1:c.1070+506_1070+520delinsCTACCTTTCAAGTCA XP_011539130.1:n.1070+506_1070+520delinsCTACCTTTCAAGTCA
XR_246241.1:n.1268+506_1268+520delinsCTACCTTTCAAGTCA
XR_246242.1:n.1252+506_1252+520delinsCTACCTTTCAAGTCA
NM_001319155.1:c.1268+506_1268+520delinsCTACCTTTCAAGTCA NP_001306084.1:n.1268+506_1268+520delinsCTACCTTTCAAGTCA
NM_001363587.1:c.1070+506_1070+520delinsCTACCTTTCAAGTCA NP_001350516.1:n.1070+506_1070+520delinsCTACCTTTCAAGTCA
NR_134988.1:n.1069+506_1069+520delinsCTACCTTTCAAGTCA
NR_134989.1:n.1260+506_1260+520delinsCTACCTTTCAAGTCA
NR_134990.1:n.1254+506_1254+520delinsCTACCTTTCAAGTCA
NR_134991.1:n.1241+506_1241+520delinsCTACCTTTCAAGTCA
NR_134992.1:n.870+506_870+520delinsCTACCTTTCAAGTCA
NR_134993.1:n.1004+506_1004+520delinsCTACCTTTCAAGTCA
NR_134994.1:n.1276+506_1276+520delinsCTACCTTTCAAGTCA
XM_017000465.1:c.1052+506_1052+520delinsCTACCTTTCAAGTCA XP_016855954.1:n.1052+506_1052+520delinsCTACCTTTCAAGTCA
XR_001737005.1:n.1342+506_1342+520delinsCTACCTTTCAAGTCA
NM_000778.4:c.1364+506_1364+520delinsCTACCTTTCAAGTCA MANE Select NP_000769.2:n.1364+506_1364+520delinsCTACCTTTCAAGTCA
NM_001319155.2:c.1268+506_1268+520delinsCTACCTTTCAAGTCA NP_001306084.1:n.1268+506_1268+520delinsCTACCTTTCAAGTCA
NM_001363587.2:c.1070+506_1070+520delinsCTACCTTTCAAGTCA NP_001350516.1:n.1070+506_1070+520delinsCTACCTTTCAAGTCA
NR_134988.2:n.1061+506_1061+520delinsCTACCTTTCAAGTCA
NR_134989.2:n.1252+506_1252+520delinsCTACCTTTCAAGTCA
NR_134990.2:n.1246+506_1246+520delinsCTACCTTTCAAGTCA
NR_134991.2:n.1233+506_1233+520delinsCTACCTTTCAAGTCA
NR_134992.2:n.862+506_862+520delinsCTACCTTTCAAGTCA
NR_134993.2:n.996+506_996+520delinsCTACCTTTCAAGTCA
NR_134994.2:n.1268+506_1268+520delinsCTACCTTTCAAGTCA