Canonical Allele Identifier: CA522613256
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1359854403
gnomAD v2: 1-47398619-G-A
gnomAD v3: 1-46932947-G-A
gnomAD v4: 1-46932947-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932947G>A , CM000663.2:g.46932947G>A GRCh38
NC_000001.10:g.47398619G>A , CM000663.1:g.47398619G>A GRCh37
NC_000001.9:g.47171206G>A NCBI36
NG_007932.1:g.13538C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1287+36C>T MANE Select ENSP00000311095.4:n.1287+36C>T
ENST00000310638.8:c.1287+36C>T ENSP00000311095.4:n.1287+36C>T
ENST00000371904.8:c.1290+36C>T ENSP00000360971.4:n.1290+36C>T
ENST00000371905.1:c.1287+36C>T ENSP00000360972.1:n.1287+36C>T
ENST00000462347.5:c.993+36C>T ENSP00000477495.1:n.993+36C>T
ENST00000465874.5:c.*85+36C>T ENSP00000476368.1:n.*85+36C>T
ENST00000468629.5:c.1127-110C>T ENSP00000476619.1:n.1127-110C>T
ENST00000474458.5:c.743-110C>T ENSP00000476988.1:n.743-110C>T
ENST00000475477.5:c.*82-110C>T ENSP00000476854.1:n.*82-110C>T
NM_000778.3:c.1287+36C>T NP_000769.2:n.1287+36C>T
XM_005270539.1:c.993+36C>T XP_005270596.1:n.993+36C>T
XM_011540826.1:c.1305+36C>T XP_011539128.1:n.1305+36C>T
XM_011540827.1:c.1011+36C>T XP_011539129.1:n.1011+36C>T
XM_011540828.1:c.993+36C>T XP_011539130.1:n.993+36C>T
XR_246241.1:n.1191+36C>T
XR_246242.1:n.1175+36C>T
NM_001319155.1:c.1191+36C>T NP_001306084.1:n.1191+36C>T
NM_001363587.1:c.993+36C>T NP_001350516.1:n.993+36C>T
NR_134988.1:n.992+36C>T
NR_134989.1:n.1183+36C>T
NR_134990.1:n.1178-110C>T
NR_134991.1:n.1164+36C>T
NR_134992.1:n.794-110C>T
NR_134993.1:n.928-110C>T
NR_134994.1:n.1199+36C>T
XM_017000465.1:c.975+36C>T XP_016855954.1:n.975+36C>T
XR_001737005.1:n.1266-110C>T
NM_000778.4:c.1287+36C>T MANE Select NP_000769.2:n.1287+36C>T
NM_001319155.2:c.1191+36C>T NP_001306084.1:n.1191+36C>T
NM_001363587.2:c.993+36C>T NP_001350516.1:n.993+36C>T
NR_134988.2:n.984+36C>T
NR_134989.2:n.1175+36C>T
NR_134990.2:n.1170-110C>T
NR_134991.2:n.1156+36C>T
NR_134992.2:n.786-110C>T
NR_134993.2:n.920-110C>T
NR_134994.2:n.1191+36C>T