Canonical Allele Identifier: CA2645485345

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46931427-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931427A>C , CM000663.2:g.46931427A>C	GRCh38
NC_000001.10:g.47397099A>C , CM000663.1:g.47397099A>C	GRCh37
NC_000001.9:g.47169686A>C	NCBI36
NG_007932.1:g.15058T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-1117T>G MANE Select	ENSP00000311095.4:n.1365-1117T>G
ENST00000310638.8:c.1365-1117T>G	ENSP00000311095.4:n.1365-1117T>G
ENST00000371904.8:c.1368-1117T>G	ENSP00000360971.4:n.1368-1117T>G
ENST00000462347.5:c.1071-1117T>G	ENSP00000477495.1:n.1071-1117T>G
ENST00000468629.5:c.*70-1117T>G	ENSP00000476619.1:n.*70-1117T>G
ENST00000474458.5:c.*70-1117T>G	ENSP00000476988.1:n.*70-1117T>G
ENST00000475477.5:c.*159-1117T>G	ENSP00000476854.1:n.*159-1117T>G
NM_000778.3:c.1365-1117T>G	NP_000769.2:n.1365-1117T>G
XM_011540826.1:c.1383-1117T>G	XP_011539128.1:n.1383-1117T>G
XM_011540827.1:c.1089-1117T>G	XP_011539129.1:n.1089-1117T>G
XM_011540828.1:c.1071-1117T>G	XP_011539130.1:n.1071-1117T>G
XR_246241.1:n.1269-1117T>G
XR_246242.1:n.1253-1117T>G
NM_001319155.1:c.1269-1117T>G	NP_001306084.1:n.1269-1117T>G
NM_001363587.1:c.1071-1117T>G	NP_001350516.1:n.1071-1117T>G
NR_134988.1:n.1070-1117T>G
NR_134989.1:n.1261-1117T>G
NR_134990.1:n.1255-1117T>G
NR_134991.1:n.1242-1117T>G
NR_134992.1:n.871-1117T>G
NR_134993.1:n.1005-1117T>G
NR_134994.1:n.1277-1117T>G
XM_017000465.1:c.1053-1117T>G	XP_016855954.1:n.1053-1117T>G
XR_001737005.1:n.1343-1117T>G
NM_000778.4:c.1365-1117T>G MANE Select	NP_000769.2:n.1365-1117T>G
NM_001319155.2:c.1269-1117T>G	NP_001306084.1:n.1269-1117T>G
NM_001363587.2:c.1071-1117T>G	NP_001350516.1:n.1071-1117T>G
NR_134988.2:n.1062-1117T>G
NR_134989.2:n.1253-1117T>G
NR_134990.2:n.1247-1117T>G
NR_134991.2:n.1234-1117T>G
NR_134992.2:n.863-1117T>G
NR_134993.2:n.997-1117T>G
NR_134994.2:n.1269-1117T>G