Canonical Allele Identifier: CA2474390697

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932994_46932995delinsGC , CM000663.2:g.46932994_46932995delinsGC	GRCh38
NC_000001.10:g.47398666_47398667delinsGC , CM000663.1:g.47398666_47398667delinsGC	GRCh37
NC_000001.9:g.47171253_47171254delinsGC	NCBI36
NG_007932.1:g.13490_13491delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1275_1276delinsGC MANE Select	ENSP00000311095.4:p.Trp425=
ENST00000310638.8:c.1275_1276delinsGC	ENSP00000311095.4:p.Trp425=
ENST00000371904.8:c.1278_1279delinsGC	ENSP00000360971.4:p.Trp426=
ENST00000371905.1:c.1275_1276delinsGC	ENSP00000360972.1:p.Trp425=
ENST00000462347.5:c.981_982delinsGC	ENSP00000477495.1:p.Trp327=
ENST00000465874.5:c.*73_*74delinsGC	ENSP00000476368.1:n.*73_*74delinsGC
ENST00000468629.5:c.1127-158_1127-157delinsGC	ENSP00000476619.1:n.1127-158_1127-157delinsGC
ENST00000474458.5:c.743-158_743-157delinsGC	ENSP00000476988.1:n.743-158_743-157delinsGC
ENST00000475477.5:c.*82-158_*82-157delinsGC	ENSP00000476854.1:n.*82-158_*82-157delinsGC
NM_000778.3:c.1275_1276delinsGC	NP_000769.2:p.Trp425=
XM_005270539.1:c.981_982delinsGC	XP_005270596.1:p.Trp327=
XM_011540826.1:c.1293_1294delinsGC	XP_011539128.1:p.Trp431=
XM_011540827.1:c.999_1000delinsGC	XP_011539129.1:p.Trp333=
XM_011540828.1:c.981_982delinsGC	XP_011539130.1:p.Trp327=
XR_246241.1:n.1179_1180delinsGC
XR_246242.1:n.1163_1164delinsGC
NM_001319155.1:c.1179_1180delinsGC	NP_001306084.1:p.Trp393=
NM_001363587.1:c.981_982delinsGC	NP_001350516.1:p.Trp327=
NR_134988.1:n.980_981delinsGC
NR_134989.1:n.1171_1172delinsGC
NR_134990.1:n.1178-158_1178-157delinsGC
NR_134991.1:n.1152_1153delinsGC
NR_134992.1:n.794-158_794-157delinsGC
NR_134993.1:n.928-158_928-157delinsGC
NR_134994.1:n.1187_1188delinsGC
XM_017000465.1:c.963_964delinsGC	XP_016855954.1:p.Trp321=
XR_001737005.1:n.1266-158_1266-157delinsGC
NM_000778.4:c.1275_1276delinsGC MANE Select	NP_000769.2:p.Trp425=
NM_001319155.2:c.1179_1180delinsGC	NP_001306084.1:p.Trp393=
NM_001363587.2:c.981_982delinsGC	NP_001350516.1:p.Trp327=
NR_134988.2:n.972_973delinsGC
NR_134989.2:n.1163_1164delinsGC
NR_134990.2:n.1170-158_1170-157delinsGC
NR_134991.2:n.1144_1145delinsGC
NR_134992.2:n.786-158_786-157delinsGC
NR_134993.2:n.920-158_920-157delinsGC
NR_134994.2:n.1179_1180delinsGC