Canonical Allele Identifier: CA417755751

Gene: CYP4A11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932772T>A , CM000663.2:g.46932772T>A	GRCh38
NC_000001.10:g.47398444T>A , CM000663.1:g.47398444T>A	GRCh37
NC_000001.9:g.47171031T>A	NCBI36
NG_007932.1:g.13713A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1353A>T MANE Select	ENSP00000311095.4:p.Ser451=
ENST00000310638.8:c.1353A>T	ENSP00000311095.4:p.Ser451=
ENST00000371904.8:c.1356A>T	ENSP00000360971.4:p.Ser452=
ENST00000371905.1:c.1353A>T	ENSP00000360972.1:p.Ser451=
ENST00000462347.5:c.1059A>T	ENSP00000477495.1:p.Ser353=
ENST00000465874.5:c.*151A>T	ENSP00000476368.1:n.*151A>T
ENST00000468629.5:c.*58A>T	ENSP00000476619.1:n.*58A>T
ENST00000474458.5:c.*58A>T	ENSP00000476988.1:n.*58A>T
ENST00000475477.5:c.*147A>T	ENSP00000476854.1:n.*147A>T
NM_000778.3:c.1353A>T	NP_000769.2:p.Ser451=
XM_005270539.1:c.1059A>T	XP_005270596.1:p.Ser353=
XM_011540826.1:c.1371A>T	XP_011539128.1:p.Ser457=
XM_011540827.1:c.1077A>T	XP_011539129.1:p.Ser359=
XM_011540828.1:c.1059A>T	XP_011539130.1:p.Ser353=
XR_246241.1:n.1257A>T
XR_246242.1:n.1241A>T
NM_001319155.1:c.1257A>T	NP_001306084.1:p.Ser419=
NM_001363587.1:c.1059A>T	NP_001350516.1:p.Ser353=
NR_134988.1:n.1058A>T
NR_134989.1:n.1249A>T
NR_134990.1:n.1243A>T
NR_134991.1:n.1230A>T
NR_134992.1:n.859A>T
NR_134993.1:n.993A>T
NR_134994.1:n.1265A>T
XM_017000465.1:c.1041A>T	XP_016855954.1:p.Ser347=
XR_001737005.1:n.1331A>T
NM_000778.4:c.1353A>T MANE Select	NP_000769.2:p.Ser451=
NM_001319155.2:c.1257A>T	NP_001306084.1:p.Ser419=
NM_001363587.2:c.1059A>T	NP_001350516.1:p.Ser353=
NR_134988.2:n.1050A>T
NR_134989.2:n.1241A>T
NR_134990.2:n.1235A>T
NR_134991.2:n.1222A>T
NR_134992.2:n.851A>T
NR_134993.2:n.985A>T
NR_134994.2:n.1257A>T