Canonical Allele Identifier: CA2645485332

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46931412-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931414del , CM000663.2:g.46931414del	GRCh38
NC_000001.10:g.47397086del , CM000663.1:g.47397086del	GRCh37
NC_000001.9:g.47169673del	NCBI36
NG_007932.1:g.15072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-1103del MANE Select	ENSP00000311095.4:n.1365-1103del
ENST00000310638.8:c.1365-1103del	ENSP00000311095.4:n.1365-1103del
ENST00000371904.8:c.1368-1103del	ENSP00000360971.4:n.1368-1103del
ENST00000462347.5:c.1071-1103del	ENSP00000477495.1:n.1071-1103del
ENST00000468629.5:c.*70-1103del	ENSP00000476619.1:n.*70-1103del
ENST00000474458.5:c.*70-1103del	ENSP00000476988.1:n.*70-1103del
ENST00000475477.5:c.*159-1103del	ENSP00000476854.1:n.*159-1103del
NM_000778.3:c.1365-1103del	NP_000769.2:n.1365-1103del
XM_011540826.1:c.1383-1103del	XP_011539128.1:n.1383-1103del
XM_011540827.1:c.1089-1103del	XP_011539129.1:n.1089-1103del
XM_011540828.1:c.1071-1103del	XP_011539130.1:n.1071-1103del
XR_246241.1:n.1269-1103del
XR_246242.1:n.1253-1103del
NM_001319155.1:c.1269-1103del	NP_001306084.1:n.1269-1103del
NM_001363587.1:c.1071-1103del	NP_001350516.1:n.1071-1103del
NR_134988.1:n.1070-1103del
NR_134989.1:n.1261-1103del
NR_134990.1:n.1255-1103del
NR_134991.1:n.1242-1103del
NR_134992.1:n.871-1103del
NR_134993.1:n.1005-1103del
NR_134994.1:n.1277-1103del
XM_017000465.1:c.1053-1103del	XP_016855954.1:n.1053-1103del
XR_001737005.1:n.1343-1103del
NM_000778.4:c.1365-1103del MANE Select	NP_000769.2:n.1365-1103del
NM_001319155.2:c.1269-1103del	NP_001306084.1:n.1269-1103del
NM_001363587.2:c.1071-1103del	NP_001350516.1:n.1071-1103del
NR_134988.2:n.1062-1103del
NR_134989.2:n.1253-1103del
NR_134990.2:n.1247-1103del
NR_134991.2:n.1234-1103del
NR_134992.2:n.863-1103del
NR_134993.2:n.997-1103del
NR_134994.2:n.1269-1103del