Canonical Allele Identifier: CA340223115
Gene: CYP4A11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46932773G>C , CM000663.2:g.46932773G>C GRCh38
NC_000001.10:g.47398445G>C , CM000663.1:g.47398445G>C GRCh37
NC_000001.9:g.47171032G>C NCBI36
NG_007932.1:g.13712C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000310638.9:c.1352C>G MANE Select ENSP00000311095.4:p.Ser451Ter
ENST00000310638.8:c.1352C>G ENSP00000311095.4:p.Ser451Ter
ENST00000371904.8:c.1355C>G ENSP00000360971.4:p.Ser452Ter
ENST00000371905.1:c.1352C>G ENSP00000360972.1:p.Ser451Ter
ENST00000462347.5:c.1058C>G ENSP00000477495.1:p.Ser353Ter
ENST00000465874.5:c.*150C>G ENSP00000476368.1:n.*150C>G
ENST00000468629.5:c.*57C>G ENSP00000476619.1:n.*57C>G
ENST00000474458.5:c.*57C>G ENSP00000476988.1:n.*57C>G
ENST00000475477.5:c.*146C>G ENSP00000476854.1:n.*146C>G
NM_000778.3:c.1352C>G NP_000769.2:p.Ser451Ter
XM_005270539.1:c.1058C>G XP_005270596.1:p.Ser353Ter
XM_011540826.1:c.1370C>G XP_011539128.1:p.Ser457Ter
XM_011540827.1:c.1076C>G XP_011539129.1:p.Ser359Ter
XM_011540828.1:c.1058C>G XP_011539130.1:p.Ser353Ter
XR_246241.1:n.1256C>G
XR_246242.1:n.1240C>G
NM_001319155.1:c.1256C>G NP_001306084.1:p.Ser419Ter
NM_001363587.1:c.1058C>G NP_001350516.1:p.Ser353Ter
NR_134988.1:n.1057C>G
NR_134989.1:n.1248C>G
NR_134990.1:n.1242C>G
NR_134991.1:n.1229C>G
NR_134992.1:n.858C>G
NR_134993.1:n.992C>G
NR_134994.1:n.1264C>G
XM_017000465.1:c.1040C>G XP_016855954.1:p.Ser347Ter
XR_001737005.1:n.1330C>G
NM_000778.4:c.1352C>G MANE Select NP_000769.2:p.Ser451Ter
NM_001319155.2:c.1256C>G NP_001306084.1:p.Ser419Ter
NM_001363587.2:c.1058C>G NP_001350516.1:p.Ser353Ter
NR_134988.2:n.1049C>G
NR_134989.2:n.1240C>G
NR_134990.2:n.1234C>G
NR_134991.2:n.1221C>G
NR_134992.2:n.850C>G
NR_134993.2:n.984C>G
NR_134994.2:n.1256C>G