Canonical Allele Identifier: CA417755743

Gene: CYP4A11

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932769T>G , CM000663.2:g.46932769T>G	GRCh38
NC_000001.10:g.47398441T>G , CM000663.1:g.47398441T>G	GRCh37
NC_000001.9:g.47171028T>G	NCBI36
NG_007932.1:g.13716A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1356A>C MANE Select	ENSP00000311095.4:p.Gly452=
ENST00000310638.8:c.1356A>C	ENSP00000311095.4:p.Gly452=
ENST00000371904.8:c.1359A>C	ENSP00000360971.4:p.Gly453=
ENST00000371905.1:c.1356A>C	ENSP00000360972.1:p.Gly452=
ENST00000462347.5:c.1062A>C	ENSP00000477495.1:p.Gly354=
ENST00000465874.5:c.*154A>C	ENSP00000476368.1:n.*154A>C
ENST00000468629.5:c.*61A>C	ENSP00000476619.1:n.*61A>C
ENST00000474458.5:c.*61A>C	ENSP00000476988.1:n.*61A>C
ENST00000475477.5:c.*150A>C	ENSP00000476854.1:n.*150A>C
NM_000778.3:c.1356A>C	NP_000769.2:p.Gly452=
XM_005270539.1:c.1062A>C	XP_005270596.1:p.Gly354=
XM_011540826.1:c.1374A>C	XP_011539128.1:p.Gly458=
XM_011540827.1:c.1080A>C	XP_011539129.1:p.Gly360=
XM_011540828.1:c.1062A>C	XP_011539130.1:p.Gly354=
XR_246241.1:n.1260A>C
XR_246242.1:n.1244A>C
NM_001319155.1:c.1260A>C	NP_001306084.1:p.Gly420=
NM_001363587.1:c.1062A>C	NP_001350516.1:p.Gly354=
NR_134988.1:n.1061A>C
NR_134989.1:n.1252A>C
NR_134990.1:n.1246A>C
NR_134991.1:n.1233A>C
NR_134992.1:n.862A>C
NR_134993.1:n.996A>C
NR_134994.1:n.1268A>C
XM_017000465.1:c.1044A>C	XP_016855954.1:p.Gly348=
XR_001737005.1:n.1334A>C
NM_000778.4:c.1356A>C MANE Select	NP_000769.2:p.Gly452=
NM_001319155.2:c.1260A>C	NP_001306084.1:p.Gly420=
NM_001363587.2:c.1062A>C	NP_001350516.1:p.Gly354=
NR_134988.2:n.1053A>C
NR_134989.2:n.1244A>C
NR_134990.2:n.1238A>C
NR_134991.2:n.1225A>C
NR_134992.2:n.854A>C
NR_134993.2:n.988A>C
NR_134994.2:n.1260A>C