Canonical Allele Identifier: CA2645486228

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932732-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932732T>G , CM000663.2:g.46932732T>G	GRCh38
NC_000001.10:g.47398404T>G , CM000663.1:g.47398404T>G	GRCh37
NC_000001.9:g.47170991T>G	NCBI36
NG_007932.1:g.13753A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364+29A>C MANE Select	ENSP00000311095.4:n.1364+29A>C
ENST00000310638.8:c.1364+29A>C	ENSP00000311095.4:n.1364+29A>C
ENST00000371904.8:c.1367+29A>C	ENSP00000360971.4:n.1367+29A>C
ENST00000371905.1:c.*25A>C	ENSP00000360972.1:n.*25A>C
ENST00000462347.5:c.1070+29A>C	ENSP00000477495.1:n.1070+29A>C
ENST00000465874.5:c.*191A>C	ENSP00000476368.1:n.*191A>C
ENST00000468629.5:c.*69+29A>C	ENSP00000476619.1:n.*69+29A>C
ENST00000474458.5:c.*69+29A>C	ENSP00000476988.1:n.*69+29A>C
ENST00000475477.5:c.*158+29A>C	ENSP00000476854.1:n.*158+29A>C
NM_000778.3:c.1364+29A>C	NP_000769.2:n.1364+29A>C
XM_011540826.1:c.1382+29A>C	XP_011539128.1:n.1382+29A>C
XM_011540827.1:c.1088+29A>C	XP_011539129.1:n.1088+29A>C
XM_011540828.1:c.1070+29A>C	XP_011539130.1:n.1070+29A>C
XR_246241.1:n.1268+29A>C
XR_246242.1:n.1252+29A>C
NM_001319155.1:c.1268+29A>C	NP_001306084.1:n.1268+29A>C
NM_001363587.1:c.1070+29A>C	NP_001350516.1:n.1070+29A>C
NR_134988.1:n.1069+29A>C
NR_134989.1:n.1260+29A>C
NR_134990.1:n.1254+29A>C
NR_134991.1:n.1241+29A>C
NR_134992.1:n.870+29A>C
NR_134993.1:n.1004+29A>C
NR_134994.1:n.1276+29A>C
XM_017000465.1:c.1052+29A>C	XP_016855954.1:n.1052+29A>C
XR_001737005.1:n.1342+29A>C
NM_000778.4:c.1364+29A>C MANE Select	NP_000769.2:n.1364+29A>C
NM_001319155.2:c.1268+29A>C	NP_001306084.1:n.1268+29A>C
NM_001363587.2:c.1070+29A>C	NP_001350516.1:n.1070+29A>C
NR_134988.2:n.1061+29A>C
NR_134989.2:n.1252+29A>C
NR_134990.2:n.1246+29A>C
NR_134991.2:n.1233+29A>C
NR_134992.2:n.862+29A>C
NR_134993.2:n.996+29A>C
NR_134994.2:n.1268+29A>C