Canonical Allele Identifier: CA2645486077

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932411-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932412del , CM000663.2:g.46932412del	GRCh38
NC_000001.10:g.47398084del , CM000663.1:g.47398084del	GRCh37
NC_000001.9:g.47170671del	NCBI36
NG_007932.1:g.14073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+349del MANE Select	ENSP00000311095.4:n.1364+349del
ENST00000310638.8:c.1364+349del	ENSP00000311095.4:n.1364+349del
ENST00000371904.8:c.1367+349del	ENSP00000360971.4:n.1367+349del
ENST00000462347.5:c.1070+349del	ENSP00000477495.1:n.1070+349del
ENST00000465874.5:c.*511del	ENSP00000476368.1:n.*511del
ENST00000468629.5:c.*69+349del	ENSP00000476619.1:n.*69+349del
ENST00000474458.5:c.*69+349del	ENSP00000476988.1:n.*69+349del
ENST00000475477.5:c.*158+349del	ENSP00000476854.1:n.*158+349del
NM_000778.3:c.1364+349del	NP_000769.2:n.1364+349del
XM_011540826.1:c.1382+349del	XP_011539128.1:n.1382+349del
XM_011540827.1:c.1088+349del	XP_011539129.1:n.1088+349del
XM_011540828.1:c.1070+349del	XP_011539130.1:n.1070+349del
XR_246241.1:n.1268+349del
XR_246242.1:n.1252+349del
NM_001319155.1:c.1268+349del	NP_001306084.1:n.1268+349del
NM_001363587.1:c.1070+349del	NP_001350516.1:n.1070+349del
NR_134988.1:n.1069+349del
NR_134989.1:n.1260+349del
NR_134990.1:n.1254+349del
NR_134991.1:n.1241+349del
NR_134992.1:n.870+349del
NR_134993.1:n.1004+349del
NR_134994.1:n.1276+349del
XM_017000465.1:c.1052+349del	XP_016855954.1:n.1052+349del
XR_001737005.1:n.1342+349del
NM_000778.4:c.1364+349del MANE Select	NP_000769.2:n.1364+349del
NM_001319155.2:c.1268+349del	NP_001306084.1:n.1268+349del
NM_001363587.2:c.1070+349del	NP_001350516.1:n.1070+349del
NR_134988.2:n.1061+349del
NR_134989.2:n.1252+349del
NR_134990.2:n.1246+349del
NR_134991.2:n.1233+349del
NR_134992.2:n.862+349del
NR_134993.2:n.996+349del
NR_134994.2:n.1268+349del