Canonical Allele Identifier: CA2474390402

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932271_46932272delinsTG , CM000663.2:g.46932271_46932272delinsTG	GRCh38
NC_000001.10:g.47397943_47397944delinsTG , CM000663.1:g.47397943_47397944delinsTG	GRCh37
NC_000001.9:g.47170530_47170531delinsTG	NCBI36
NG_007932.1:g.14213_14214delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+489_1364+490delinsCA MANE Select	ENSP00000311095.4:n.1364+489_1364+490delinsCA
ENST00000310638.8:c.1364+489_1364+490delinsCA	ENSP00000311095.4:n.1364+489_1364+490delinsCA
ENST00000371904.8:c.1367+489_1367+490delinsCA	ENSP00000360971.4:n.1367+489_1367+490delinsCA
ENST00000462347.5:c.1070+489_1070+490delinsCA	ENSP00000477495.1:n.1070+489_1070+490delinsCA
ENST00000465874.5:c.*651_*652delinsCA	ENSP00000476368.1:n.*651_*652delinsCA
ENST00000468629.5:c.*69+489_*69+490delinsCA	ENSP00000476619.1:n.*69+489_*69+490delinsCA
ENST00000474458.5:c.*69+489_*69+490delinsCA	ENSP00000476988.1:n.*69+489_*69+490delinsCA
ENST00000475477.5:c.*158+489_*158+490delinsCA	ENSP00000476854.1:n.*158+489_*158+490delinsCA
NM_000778.3:c.1364+489_1364+490delinsCA	NP_000769.2:n.1364+489_1364+490delinsCA
XM_011540826.1:c.1382+489_1382+490delinsCA	XP_011539128.1:n.1382+489_1382+490delinsCA
XM_011540827.1:c.1088+489_1088+490delinsCA	XP_011539129.1:n.1088+489_1088+490delinsCA
XM_011540828.1:c.1070+489_1070+490delinsCA	XP_011539130.1:n.1070+489_1070+490delinsCA
XR_246241.1:n.1268+489_1268+490delinsCA
XR_246242.1:n.1252+489_1252+490delinsCA
NM_001319155.1:c.1268+489_1268+490delinsCA	NP_001306084.1:n.1268+489_1268+490delinsCA
NM_001363587.1:c.1070+489_1070+490delinsCA	NP_001350516.1:n.1070+489_1070+490delinsCA
NR_134988.1:n.1069+489_1069+490delinsCA
NR_134989.1:n.1260+489_1260+490delinsCA
NR_134990.1:n.1254+489_1254+490delinsCA
NR_134991.1:n.1241+489_1241+490delinsCA
NR_134992.1:n.870+489_870+490delinsCA
NR_134993.1:n.1004+489_1004+490delinsCA
NR_134994.1:n.1276+489_1276+490delinsCA
XM_017000465.1:c.1052+489_1052+490delinsCA	XP_016855954.1:n.1052+489_1052+490delinsCA
XR_001737005.1:n.1342+489_1342+490delinsCA
NM_000778.4:c.1364+489_1364+490delinsCA MANE Select	NP_000769.2:n.1364+489_1364+490delinsCA
NM_001319155.2:c.1268+489_1268+490delinsCA	NP_001306084.1:n.1268+489_1268+490delinsCA
NM_001363587.2:c.1070+489_1070+490delinsCA	NP_001350516.1:n.1070+489_1070+490delinsCA
NR_134988.2:n.1061+489_1061+490delinsCA
NR_134989.2:n.1252+489_1252+490delinsCA
NR_134990.2:n.1246+489_1246+490delinsCA
NR_134991.2:n.1233+489_1233+490delinsCA
NR_134992.2:n.862+489_862+490delinsCA
NR_134993.2:n.996+489_996+490delinsCA
NR_134994.2:n.1268+489_1268+490delinsCA