Canonical Allele Identifier: CA2474390786

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1681138999

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933191_46933192insCCACAGGTATCAT , CM000663.2:g.46933191_46933192insCCACAGGTATCAT	GRCh38
NC_000001.10:g.47398863_47398864insCCACAGGTATCAT , CM000663.1:g.47398863_47398864insCCACAGGTATCAT	GRCh37
NC_000001.9:g.47171450_47171451insCCACAGGTATCAT	NCBI36
NG_007932.1:g.13293_13294insATGATACCTGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-145_1223-144insATGATACCTGTGG MANE Select	ENSP00000311095.4:n.1223-145_1223-144insATGATACCTGTGG
ENST00000310638.8:c.1223-145_1223-144insATGATACCTGTGG	ENSP00000311095.4:n.1223-145_1223-144insATGATACCTGTGG
ENST00000371904.8:c.1226-145_1226-144insATGATACCTGTGG	ENSP00000360971.4:n.1226-145_1226-144insATGATACCTGTGG
ENST00000371905.1:c.1223-145_1223-144insATGATACCTGTGG	ENSP00000360972.1:n.1223-145_1223-144insATGATACCTGTGG
ENST00000462347.5:c.929-145_929-144insATGATACCTGTGG	ENSP00000477495.1:n.929-145_929-144insATGATACCTGTGG
ENST00000465874.5:c.*21-145_*21-144insATGATACCTGTGG	ENSP00000476368.1:n.*21-145_*21-144insATGATACCTGTGG
ENST00000468629.5:c.1127-355_1127-354insATGATACCTGTGG	ENSP00000476619.1:n.1127-355_1127-354insATGATACCTGTGG
ENST00000474458.5:c.743-355_743-354insATGATACCTGTGG	ENSP00000476988.1:n.743-355_743-354insATGATACCTGTGG
ENST00000475477.5:c.*82-355_*82-354insATGATACCTGTGG	ENSP00000476854.1:n.*82-355_*82-354insATGATACCTGTGG
NM_000778.3:c.1223-145_1223-144insATGATACCTGTGG	NP_000769.2:n.1223-145_1223-144insATGATACCTGTGG
XM_005270539.1:c.929-145_929-144insATGATACCTGTGG	XP_005270596.1:n.929-145_929-144insATGATACCTGTGG
XM_011540826.1:c.1241-145_1241-144insATGATACCTGTGG	XP_011539128.1:n.1241-145_1241-144insATGATACCTGTGG
XM_011540827.1:c.947-145_947-144insATGATACCTGTGG	XP_011539129.1:n.947-145_947-144insATGATACCTGTGG
XM_011540828.1:c.929-145_929-144insATGATACCTGTGG	XP_011539130.1:n.929-145_929-144insATGATACCTGTGG
XR_246241.1:n.1127-145_1127-144insATGATACCTGTGG
XR_246242.1:n.1111-145_1111-144insATGATACCTGTGG
NM_001319155.1:c.1127-145_1127-144insATGATACCTGTGG	NP_001306084.1:n.1127-145_1127-144insATGATACCTGTGG
NM_001363587.1:c.929-145_929-144insATGATACCTGTGG	NP_001350516.1:n.929-145_929-144insATGATACCTGTGG
NR_134988.1:n.928-145_928-144insATGATACCTGTGG
NR_134989.1:n.1119-145_1119-144insATGATACCTGTGG
NR_134990.1:n.1178-355_1178-354insATGATACCTGTGG
NR_134991.1:n.1100-145_1100-144insATGATACCTGTGG
NR_134992.1:n.794-355_794-354insATGATACCTGTGG
NR_134993.1:n.928-355_928-354insATGATACCTGTGG
NR_134994.1:n.1135-145_1135-144insATGATACCTGTGG
XM_017000465.1:c.911-145_911-144insATGATACCTGTGG	XP_016855954.1:n.911-145_911-144insATGATACCTGTGG
XR_001737005.1:n.1266-355_1266-354insATGATACCTGTGG
NM_000778.4:c.1223-145_1223-144insATGATACCTGTGG MANE Select	NP_000769.2:n.1223-145_1223-144insATGATACCTGTGG
NM_001319155.2:c.1127-145_1127-144insATGATACCTGTGG	NP_001306084.1:n.1127-145_1127-144insATGATACCTGTGG
NM_001363587.2:c.929-145_929-144insATGATACCTGTGG	NP_001350516.1:n.929-145_929-144insATGATACCTGTGG
NR_134988.2:n.920-145_920-144insATGATACCTGTGG
NR_134989.2:n.1111-145_1111-144insATGATACCTGTGG
NR_134990.2:n.1170-355_1170-354insATGATACCTGTGG
NR_134991.2:n.1092-145_1092-144insATGATACCTGTGG
NR_134992.2:n.786-355_786-354insATGATACCTGTGG
NR_134993.2:n.920-355_920-354insATGATACCTGTGG
NR_134994.2:n.1127-145_1127-144insATGATACCTGTGG