Canonical Allele Identifier: CA522613254
Gene: CYP4A11 HGNC NCBI

Linked Data

dbSNP Id: rs1414646497
gnomAD v2: 1-47398614-T-C
gnomAD v4: 1-46932942-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932942T>C , CM000663.2:g.46932942T>C GRCh38
NC_000001.10:g.47398614T>C , CM000663.1:g.47398614T>C GRCh37
NC_000001.9:g.47171201T>C NCBI36
NG_007932.1:g.13543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000310638.9:c.1287+41A>G MANE Select ENSP00000311095.4:n.1287+41A>G
ENST00000310638.8:c.1287+41A>G ENSP00000311095.4:n.1287+41A>G
ENST00000371904.8:c.1290+41A>G ENSP00000360971.4:n.1290+41A>G
ENST00000371905.1:c.1287+41A>G ENSP00000360972.1:n.1287+41A>G
ENST00000462347.5:c.993+41A>G ENSP00000477495.1:n.993+41A>G
ENST00000465874.5:c.*85+41A>G ENSP00000476368.1:n.*85+41A>G
ENST00000468629.5:c.1127-105A>G ENSP00000476619.1:n.1127-105A>G
ENST00000474458.5:c.743-105A>G ENSP00000476988.1:n.743-105A>G
ENST00000475477.5:c.*82-105A>G ENSP00000476854.1:n.*82-105A>G
NM_000778.3:c.1287+41A>G NP_000769.2:n.1287+41A>G
XM_005270539.1:c.993+41A>G XP_005270596.1:n.993+41A>G
XM_011540826.1:c.1305+41A>G XP_011539128.1:n.1305+41A>G
XM_011540827.1:c.1011+41A>G XP_011539129.1:n.1011+41A>G
XM_011540828.1:c.993+41A>G XP_011539130.1:n.993+41A>G
XR_246241.1:n.1191+41A>G
XR_246242.1:n.1175+41A>G
NM_001319155.1:c.1191+41A>G NP_001306084.1:n.1191+41A>G
NM_001363587.1:c.993+41A>G NP_001350516.1:n.993+41A>G
NR_134988.1:n.992+41A>G
NR_134989.1:n.1183+41A>G
NR_134990.1:n.1178-105A>G
NR_134991.1:n.1164+41A>G
NR_134992.1:n.794-105A>G
NR_134993.1:n.928-105A>G
NR_134994.1:n.1199+41A>G
XM_017000465.1:c.975+41A>G XP_016855954.1:n.975+41A>G
XR_001737005.1:n.1266-105A>G
NM_000778.4:c.1287+41A>G MANE Select NP_000769.2:n.1287+41A>G
NM_001319155.2:c.1191+41A>G NP_001306084.1:n.1191+41A>G
NM_001363587.2:c.993+41A>G NP_001350516.1:n.993+41A>G
NR_134988.2:n.984+41A>G
NR_134989.2:n.1175+41A>G
NR_134990.2:n.1170-105A>G
NR_134991.2:n.1156+41A>G
NR_134992.2:n.786-105A>G
NR_134993.2:n.920-105A>G
NR_134994.2:n.1191+41A>G