Canonical Allele Identifier: CA2645486186

Gene: CYP4A11

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932634C>A , CM000663.2:g.46932634C>A	GRCh38
NC_000001.10:g.47398306C>A , CM000663.1:g.47398306C>A	GRCh37
NC_000001.9:g.47170893C>A	NCBI36
NG_007932.1:g.13851G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+127G>T MANE Select	ENSP00000311095.4:n.1364+127G>T
ENST00000310638.8:c.1364+127G>T	ENSP00000311095.4:n.1364+127G>T
ENST00000371904.8:c.1367+127G>T	ENSP00000360971.4:n.1367+127G>T
ENST00000371905.1:c.*123G>T	ENSP00000360972.1:n.*123G>T
ENST00000462347.5:c.1070+127G>T	ENSP00000477495.1:n.1070+127G>T
ENST00000465874.5:c.*289G>T	ENSP00000476368.1:n.*289G>T
ENST00000468629.5:c.*69+127G>T	ENSP00000476619.1:n.*69+127G>T
ENST00000474458.5:c.*69+127G>T	ENSP00000476988.1:n.*69+127G>T
ENST00000475477.5:c.*158+127G>T	ENSP00000476854.1:n.*158+127G>T
NM_000778.3:c.1364+127G>T	NP_000769.2:n.1364+127G>T
XM_011540826.1:c.1382+127G>T	XP_011539128.1:n.1382+127G>T
XM_011540827.1:c.1088+127G>T	XP_011539129.1:n.1088+127G>T
XM_011540828.1:c.1070+127G>T	XP_011539130.1:n.1070+127G>T
XR_246241.1:n.1268+127G>T
XR_246242.1:n.1252+127G>T
NM_001319155.1:c.1268+127G>T	NP_001306084.1:n.1268+127G>T
NM_001363587.1:c.1070+127G>T	NP_001350516.1:n.1070+127G>T
NR_134988.1:n.1069+127G>T
NR_134989.1:n.1260+127G>T
NR_134990.1:n.1254+127G>T
NR_134991.1:n.1241+127G>T
NR_134992.1:n.870+127G>T
NR_134993.1:n.1004+127G>T
NR_134994.1:n.1276+127G>T
XM_017000465.1:c.1052+127G>T	XP_016855954.1:n.1052+127G>T
XR_001737005.1:n.1342+127G>T
NM_000778.4:c.1364+127G>T MANE Select	NP_000769.2:n.1364+127G>T
NM_001319155.2:c.1268+127G>T	NP_001306084.1:n.1268+127G>T
NM_001363587.2:c.1070+127G>T	NP_001350516.1:n.1070+127G>T
NR_134988.2:n.1061+127G>T
NR_134989.2:n.1252+127G>T
NR_134990.2:n.1246+127G>T
NR_134991.2:n.1233+127G>T
NR_134992.2:n.862+127G>T
NR_134993.2:n.996+127G>T
NR_134994.2:n.1268+127G>T