Canonical Allele Identifier: CA2474390752

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933122_46933123delinsCA , CM000663.2:g.46933122_46933123delinsCA	GRCh38
NC_000001.10:g.47398794_47398795delinsCA , CM000663.1:g.47398794_47398795delinsCA	GRCh37
NC_000001.9:g.47171381_47171382delinsCA	NCBI36
NG_007932.1:g.13362_13363delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-76_1223-75delinsTG MANE Select	ENSP00000311095.4:n.1223-76_1223-75delinsTG
ENST00000310638.8:c.1223-76_1223-75delinsTG	ENSP00000311095.4:n.1223-76_1223-75delinsTG
ENST00000371904.8:c.1226-76_1226-75delinsTG	ENSP00000360971.4:n.1226-76_1226-75delinsTG
ENST00000371905.1:c.1223-76_1223-75delinsTG	ENSP00000360972.1:n.1223-76_1223-75delinsTG
ENST00000462347.5:c.929-76_929-75delinsTG	ENSP00000477495.1:n.929-76_929-75delinsTG
ENST00000465874.5:c.*21-76_*21-75delinsTG	ENSP00000476368.1:n.*21-76_*21-75delinsTG
ENST00000468629.5:c.1127-286_1127-285delinsTG	ENSP00000476619.1:n.1127-286_1127-285delinsTG
ENST00000474458.5:c.743-286_743-285delinsTG	ENSP00000476988.1:n.743-286_743-285delinsTG
ENST00000475477.5:c.*82-286_*82-285delinsTG	ENSP00000476854.1:n.*82-286_*82-285delinsTG
NM_000778.3:c.1223-76_1223-75delinsTG	NP_000769.2:n.1223-76_1223-75delinsTG
XM_005270539.1:c.929-76_929-75delinsTG	XP_005270596.1:n.929-76_929-75delinsTG
XM_011540826.1:c.1241-76_1241-75delinsTG	XP_011539128.1:n.1241-76_1241-75delinsTG
XM_011540827.1:c.947-76_947-75delinsTG	XP_011539129.1:n.947-76_947-75delinsTG
XM_011540828.1:c.929-76_929-75delinsTG	XP_011539130.1:n.929-76_929-75delinsTG
XR_246241.1:n.1127-76_1127-75delinsTG
XR_246242.1:n.1111-76_1111-75delinsTG
NM_001319155.1:c.1127-76_1127-75delinsTG	NP_001306084.1:n.1127-76_1127-75delinsTG
NM_001363587.1:c.929-76_929-75delinsTG	NP_001350516.1:n.929-76_929-75delinsTG
NR_134988.1:n.928-76_928-75delinsTG
NR_134989.1:n.1119-76_1119-75delinsTG
NR_134990.1:n.1178-286_1178-285delinsTG
NR_134991.1:n.1100-76_1100-75delinsTG
NR_134992.1:n.794-286_794-285delinsTG
NR_134993.1:n.928-286_928-285delinsTG
NR_134994.1:n.1135-76_1135-75delinsTG
XM_017000465.1:c.911-76_911-75delinsTG	XP_016855954.1:n.911-76_911-75delinsTG
XR_001737005.1:n.1266-286_1266-285delinsTG
NM_000778.4:c.1223-76_1223-75delinsTG MANE Select	NP_000769.2:n.1223-76_1223-75delinsTG
NM_001319155.2:c.1127-76_1127-75delinsTG	NP_001306084.1:n.1127-76_1127-75delinsTG
NM_001363587.2:c.929-76_929-75delinsTG	NP_001350516.1:n.929-76_929-75delinsTG
NR_134988.2:n.920-76_920-75delinsTG
NR_134989.2:n.1111-76_1111-75delinsTG
NR_134990.2:n.1170-286_1170-285delinsTG
NR_134991.2:n.1092-76_1092-75delinsTG
NR_134992.2:n.786-286_786-285delinsTG
NR_134993.2:n.920-286_920-285delinsTG
NR_134994.2:n.1127-76_1127-75delinsTG