Canonical Allele Identifier: CA21988166

Gene: CYP4A11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932660C>A , CM000663.2:g.46932660C>A	GRCh38
NC_000001.10:g.47398332C>A , CM000663.1:g.47398332C>A	GRCh37
NC_000001.9:g.47170919C>A	NCBI36
NG_007932.1:g.13825G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+101G>T MANE Select	ENSP00000311095.4:n.1364+101G>T
ENST00000310638.8:c.1364+101G>T	ENSP00000311095.4:n.1364+101G>T
ENST00000371904.8:c.1367+101G>T	ENSP00000360971.4:n.1367+101G>T
ENST00000371905.1:c.*97G>T	ENSP00000360972.1:n.*97G>T
ENST00000462347.5:c.1070+101G>T	ENSP00000477495.1:n.1070+101G>T
ENST00000465874.5:c.*263G>T	ENSP00000476368.1:n.*263G>T
ENST00000468629.5:c.*69+101G>T	ENSP00000476619.1:n.*69+101G>T
ENST00000474458.5:c.*69+101G>T	ENSP00000476988.1:n.*69+101G>T
ENST00000475477.5:c.*158+101G>T	ENSP00000476854.1:n.*158+101G>T
NM_000778.3:c.1364+101G>T	NP_000769.2:n.1364+101G>T
XM_011540826.1:c.1382+101G>T	XP_011539128.1:n.1382+101G>T
XM_011540827.1:c.1088+101G>T	XP_011539129.1:n.1088+101G>T
XM_011540828.1:c.1070+101G>T	XP_011539130.1:n.1070+101G>T
XR_246241.1:n.1268+101G>T
XR_246242.1:n.1252+101G>T
NM_001319155.1:c.1268+101G>T	NP_001306084.1:n.1268+101G>T
NM_001363587.1:c.1070+101G>T	NP_001350516.1:n.1070+101G>T
NR_134988.1:n.1069+101G>T
NR_134989.1:n.1260+101G>T
NR_134990.1:n.1254+101G>T
NR_134991.1:n.1241+101G>T
NR_134992.1:n.870+101G>T
NR_134993.1:n.1004+101G>T
NR_134994.1:n.1276+101G>T
XM_017000465.1:c.1052+101G>T	XP_016855954.1:n.1052+101G>T
XR_001737005.1:n.1342+101G>T
NM_000778.4:c.1364+101G>T MANE Select	NP_000769.2:n.1364+101G>T
NM_001319155.2:c.1268+101G>T	NP_001306084.1:n.1268+101G>T
NM_001363587.2:c.1070+101G>T	NP_001350516.1:n.1070+101G>T
NR_134988.2:n.1061+101G>T
NR_134989.2:n.1252+101G>T
NR_134990.2:n.1246+101G>T
NR_134991.2:n.1233+101G>T
NR_134992.2:n.862+101G>T
NR_134993.2:n.996+101G>T
NR_134994.2:n.1268+101G>T