Canonical Allele Identifier: CA2645486096

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932450-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932450T>C , CM000663.2:g.46932450T>C	GRCh38
NC_000001.10:g.47398122T>C , CM000663.1:g.47398122T>C	GRCh37
NC_000001.9:g.47170709T>C	NCBI36
NG_007932.1:g.14035A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+311A>G MANE Select	ENSP00000311095.4:n.1364+311A>G
ENST00000310638.8:c.1364+311A>G	ENSP00000311095.4:n.1364+311A>G
ENST00000371904.8:c.1367+311A>G	ENSP00000360971.4:n.1367+311A>G
ENST00000371905.1:c.*307A>G	ENSP00000360972.1:n.*307A>G
ENST00000462347.5:c.1070+311A>G	ENSP00000477495.1:n.1070+311A>G
ENST00000465874.5:c.*473A>G	ENSP00000476368.1:n.*473A>G
ENST00000468629.5:c.*69+311A>G	ENSP00000476619.1:n.*69+311A>G
ENST00000474458.5:c.*69+311A>G	ENSP00000476988.1:n.*69+311A>G
ENST00000475477.5:c.*158+311A>G	ENSP00000476854.1:n.*158+311A>G
NM_000778.3:c.1364+311A>G	NP_000769.2:n.1364+311A>G
XM_011540826.1:c.1382+311A>G	XP_011539128.1:n.1382+311A>G
XM_011540827.1:c.1088+311A>G	XP_011539129.1:n.1088+311A>G
XM_011540828.1:c.1070+311A>G	XP_011539130.1:n.1070+311A>G
XR_246241.1:n.1268+311A>G
XR_246242.1:n.1252+311A>G
NM_001319155.1:c.1268+311A>G	NP_001306084.1:n.1268+311A>G
NM_001363587.1:c.1070+311A>G	NP_001350516.1:n.1070+311A>G
NR_134988.1:n.1069+311A>G
NR_134989.1:n.1260+311A>G
NR_134990.1:n.1254+311A>G
NR_134991.1:n.1241+311A>G
NR_134992.1:n.870+311A>G
NR_134993.1:n.1004+311A>G
NR_134994.1:n.1276+311A>G
XM_017000465.1:c.1052+311A>G	XP_016855954.1:n.1052+311A>G
XR_001737005.1:n.1342+311A>G
NM_000778.4:c.1364+311A>G MANE Select	NP_000769.2:n.1364+311A>G
NM_001319155.2:c.1268+311A>G	NP_001306084.1:n.1268+311A>G
NM_001363587.2:c.1070+311A>G	NP_001350516.1:n.1070+311A>G
NR_134988.2:n.1061+311A>G
NR_134989.2:n.1252+311A>G
NR_134990.2:n.1246+311A>G
NR_134991.2:n.1233+311A>G
NR_134992.2:n.862+311A>G
NR_134993.2:n.996+311A>G
NR_134994.2:n.1268+311A>G