Canonical Allele Identifier: CA736355337
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1422590874
gnomAD v4: 1-46932900-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932900G>A , CM000663.2:g.46932900G>A GRCh38
NC_000001.10:g.47398572G>A , CM000663.1:g.47398572G>A GRCh37
NC_000001.9:g.47171159G>A NCBI36
NG_007932.1:g.13585C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1288-63C>T MANE Select ENSP00000311095.4:n.1288-63C>T
ENST00000310638.8:c.1288-63C>T ENSP00000311095.4:n.1288-63C>T
ENST00000371904.8:c.1291-63C>T ENSP00000360971.4:n.1291-63C>T
ENST00000371905.1:c.1288-63C>T ENSP00000360972.1:n.1288-63C>T
ENST00000462347.5:c.994-63C>T ENSP00000477495.1:n.994-63C>T
ENST00000465874.5:c.*86-63C>T ENSP00000476368.1:n.*86-63C>T
ENST00000468629.5:c.1127-63C>T ENSP00000476619.1:n.1127-63C>T
ENST00000474458.5:c.743-63C>T ENSP00000476988.1:n.743-63C>T
ENST00000475477.5:c.*82-63C>T ENSP00000476854.1:n.*82-63C>T
NM_000778.3:c.1288-63C>T NP_000769.2:n.1288-63C>T
XM_005270539.1:c.994-63C>T XP_005270596.1:n.994-63C>T
XM_011540826.1:c.1306-63C>T XP_011539128.1:n.1306-63C>T
XM_011540827.1:c.1012-63C>T XP_011539129.1:n.1012-63C>T
XM_011540828.1:c.994-63C>T XP_011539130.1:n.994-63C>T
XR_246241.1:n.1192-63C>T
XR_246242.1:n.1176-63C>T
NM_001319155.1:c.1192-63C>T NP_001306084.1:n.1192-63C>T
NM_001363587.1:c.994-63C>T NP_001350516.1:n.994-63C>T
NR_134988.1:n.993-63C>T
NR_134989.1:n.1184-63C>T
NR_134990.1:n.1178-63C>T
NR_134991.1:n.1165-63C>T
NR_134992.1:n.794-63C>T
NR_134993.1:n.928-63C>T
NR_134994.1:n.1200-63C>T
XM_017000465.1:c.976-63C>T XP_016855954.1:n.976-63C>T
XR_001737005.1:n.1266-63C>T
NM_000778.4:c.1288-63C>T MANE Select NP_000769.2:n.1288-63C>T
NM_001319155.2:c.1192-63C>T NP_001306084.1:n.1192-63C>T
NM_001363587.2:c.994-63C>T NP_001350516.1:n.994-63C>T
NR_134988.2:n.985-63C>T
NR_134989.2:n.1176-63C>T
NR_134990.2:n.1170-63C>T
NR_134991.2:n.1157-63C>T
NR_134992.2:n.786-63C>T
NR_134993.2:n.920-63C>T
NR_134994.2:n.1192-63C>T