Canonical Allele Identifier: CA646048194

Gene: CYP4A11

Linked Data

• COSMIC: COSN507844

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932750G>A , CM000663.2:g.46932750G>A	GRCh38
NC_000001.10:g.47398422G>A , CM000663.1:g.47398422G>A	GRCh37
NC_000001.9:g.47171009G>A	NCBI36
NG_007932.1:g.13735C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364+11C>T MANE Select	ENSP00000311095.4:n.1364+11C>T
ENST00000310638.8:c.1364+11C>T	ENSP00000311095.4:n.1364+11C>T
ENST00000371904.8:c.1367+11C>T	ENSP00000360971.4:n.1367+11C>T
ENST00000371905.1:c.*7C>T	ENSP00000360972.1:n.*7C>T
ENST00000462347.5:c.1070+11C>T	ENSP00000477495.1:n.1070+11C>T
ENST00000465874.5:c.*173C>T	ENSP00000476368.1:n.*173C>T
ENST00000468629.5:c.*69+11C>T	ENSP00000476619.1:n.*69+11C>T
ENST00000474458.5:c.*69+11C>T	ENSP00000476988.1:n.*69+11C>T
ENST00000475477.5:c.*158+11C>T	ENSP00000476854.1:n.*158+11C>T
NM_000778.3:c.1364+11C>T	NP_000769.2:n.1364+11C>T
XM_011540826.1:c.1382+11C>T	XP_011539128.1:n.1382+11C>T
XM_011540827.1:c.1088+11C>T	XP_011539129.1:n.1088+11C>T
XM_011540828.1:c.1070+11C>T	XP_011539130.1:n.1070+11C>T
XR_246241.1:n.1268+11C>T
XR_246242.1:n.1252+11C>T
NM_001319155.1:c.1268+11C>T	NP_001306084.1:n.1268+11C>T
NM_001363587.1:c.1070+11C>T	NP_001350516.1:n.1070+11C>T
NR_134988.1:n.1069+11C>T
NR_134989.1:n.1260+11C>T
NR_134990.1:n.1254+11C>T
NR_134991.1:n.1241+11C>T
NR_134992.1:n.870+11C>T
NR_134993.1:n.1004+11C>T
NR_134994.1:n.1276+11C>T
XM_017000465.1:c.1052+11C>T	XP_016855954.1:n.1052+11C>T
XR_001737005.1:n.1342+11C>T
NM_000778.4:c.1364+11C>T MANE Select	NP_000769.2:n.1364+11C>T
NM_001319155.2:c.1268+11C>T	NP_001306084.1:n.1268+11C>T
NM_001363587.2:c.1070+11C>T	NP_001350516.1:n.1070+11C>T
NR_134988.2:n.1061+11C>T
NR_134989.2:n.1252+11C>T
NR_134990.2:n.1246+11C>T
NR_134991.2:n.1233+11C>T
NR_134992.2:n.862+11C>T
NR_134993.2:n.996+11C>T
NR_134994.2:n.1268+11C>T