Canonical Allele Identifier: CA340223109

Gene: CYP4A11

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932770C>G , CM000663.2:g.46932770C>G	GRCh38
NC_000001.10:g.47398442C>G , CM000663.1:g.47398442C>G	GRCh37
NC_000001.9:g.47171029C>G	NCBI36
NG_007932.1:g.13715G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1355G>C MANE Select	ENSP00000311095.4:p.Gly452Ala
ENST00000310638.8:c.1355G>C	ENSP00000311095.4:p.Gly452Ala
ENST00000371904.8:c.1358G>C	ENSP00000360971.4:p.Gly453Ala
ENST00000371905.1:c.1355G>C	ENSP00000360972.1:p.Gly452Ala
ENST00000462347.5:c.1061G>C	ENSP00000477495.1:p.Gly354Ala
ENST00000465874.5:c.*153G>C	ENSP00000476368.1:n.*153G>C
ENST00000468629.5:c.*60G>C	ENSP00000476619.1:n.*60G>C
ENST00000474458.5:c.*60G>C	ENSP00000476988.1:n.*60G>C
ENST00000475477.5:c.*149G>C	ENSP00000476854.1:n.*149G>C
NM_000778.3:c.1355G>C	NP_000769.2:p.Gly452Ala
XM_005270539.1:c.1061G>C	XP_005270596.1:p.Gly354Ala
XM_011540826.1:c.1373G>C	XP_011539128.1:p.Gly458Ala
XM_011540827.1:c.1079G>C	XP_011539129.1:p.Gly360Ala
XM_011540828.1:c.1061G>C	XP_011539130.1:p.Gly354Ala
XR_246241.1:n.1259G>C
XR_246242.1:n.1243G>C
NM_001319155.1:c.1259G>C	NP_001306084.1:p.Gly420Ala
NM_001363587.1:c.1061G>C	NP_001350516.1:p.Gly354Ala
NR_134988.1:n.1060G>C
NR_134989.1:n.1251G>C
NR_134990.1:n.1245G>C
NR_134991.1:n.1232G>C
NR_134992.1:n.861G>C
NR_134993.1:n.995G>C
NR_134994.1:n.1267G>C
XM_017000465.1:c.1043G>C	XP_016855954.1:p.Gly348Ala
XR_001737005.1:n.1333G>C
NM_000778.4:c.1355G>C MANE Select	NP_000769.2:p.Gly452Ala
NM_001319155.2:c.1259G>C	NP_001306084.1:p.Gly420Ala
NM_001363587.2:c.1061G>C	NP_001350516.1:p.Gly354Ala
NR_134988.2:n.1052G>C
NR_134989.2:n.1243G>C
NR_134990.2:n.1237G>C
NR_134991.2:n.1224G>C
NR_134992.2:n.853G>C
NR_134993.2:n.987G>C
NR_134994.2:n.1259G>C