Canonical Allele Identifier: CA839267
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs748946379
gnomAD v2: 1-47398419-A-C
gnomAD v4: 1-46932747-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932747A>C , CM000663.2:g.46932747A>C GRCh38
NC_000001.10:g.47398419A>C , CM000663.1:g.47398419A>C GRCh37
NC_000001.9:g.47171006A>C NCBI36
NG_007932.1:g.13738T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1364+14T>G MANE Select ENSP00000311095.4:n.1364+14T>G
ENST00000310638.8:c.1364+14T>G ENSP00000311095.4:n.1364+14T>G
ENST00000371904.8:c.1367+14T>G ENSP00000360971.4:n.1367+14T>G
ENST00000371905.1:c.*10T>G ENSP00000360972.1:n.*10T>G
ENST00000462347.5:c.1070+14T>G ENSP00000477495.1:n.1070+14T>G
ENST00000465874.5:c.*176T>G ENSP00000476368.1:n.*176T>G
ENST00000468629.5:c.*69+14T>G ENSP00000476619.1:n.*69+14T>G
ENST00000474458.5:c.*69+14T>G ENSP00000476988.1:n.*69+14T>G
ENST00000475477.5:c.*158+14T>G ENSP00000476854.1:n.*158+14T>G
NM_000778.3:c.1364+14T>G NP_000769.2:n.1364+14T>G
XM_011540826.1:c.1382+14T>G XP_011539128.1:n.1382+14T>G
XM_011540827.1:c.1088+14T>G XP_011539129.1:n.1088+14T>G
XM_011540828.1:c.1070+14T>G XP_011539130.1:n.1070+14T>G
XR_246241.1:n.1268+14T>G
XR_246242.1:n.1252+14T>G
NM_001319155.1:c.1268+14T>G NP_001306084.1:n.1268+14T>G
NM_001363587.1:c.1070+14T>G NP_001350516.1:n.1070+14T>G
NR_134988.1:n.1069+14T>G
NR_134989.1:n.1260+14T>G
NR_134990.1:n.1254+14T>G
NR_134991.1:n.1241+14T>G
NR_134992.1:n.870+14T>G
NR_134993.1:n.1004+14T>G
NR_134994.1:n.1276+14T>G
XM_017000465.1:c.1052+14T>G XP_016855954.1:n.1052+14T>G
XR_001737005.1:n.1342+14T>G
NM_000778.4:c.1364+14T>G MANE Select NP_000769.2:n.1364+14T>G
NM_001319155.2:c.1268+14T>G NP_001306084.1:n.1268+14T>G
NM_001363587.2:c.1070+14T>G NP_001350516.1:n.1070+14T>G
NR_134988.2:n.1061+14T>G
NR_134989.2:n.1252+14T>G
NR_134990.2:n.1246+14T>G
NR_134991.2:n.1233+14T>G
NR_134992.2:n.862+14T>G
NR_134993.2:n.996+14T>G
NR_134994.2:n.1268+14T>G