Canonical Allele Identifier: CA2474390607

Gene: CYP4A11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932813G= , CM000663.2:g.46932813G=	GRCh38
NC_000001.10:g.47398485G= , CM000663.1:g.47398485G=	GRCh37
NC_000001.9:g.47171072G=	NCBI36
NG_007932.1:g.13672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1312C= MANE Select	ENSP00000311095.4:p.Pro438=
ENST00000310638.8:c.1312C=	ENSP00000311095.4:p.Pro438=
ENST00000371904.8:c.1315C=	ENSP00000360971.4:p.Pro439=
ENST00000371905.1:c.1312C=	ENSP00000360972.1:p.Pro438=
ENST00000462347.5:c.1018C=	ENSP00000477495.1:p.Pro340=
ENST00000465874.5:c.*110C=	ENSP00000476368.1:n.*110C=
ENST00000468629.5:c.*17C=	ENSP00000476619.1:n.*17C=
ENST00000474458.5:c.*17C=	ENSP00000476988.1:n.*17C=
ENST00000475477.5:c.*106C=	ENSP00000476854.1:n.*106C=
NM_000778.3:c.1312C=	NP_000769.2:p.Pro438=
XM_005270539.1:c.1018C=	XP_005270596.1:p.Pro340=
XM_011540826.1:c.1330C=	XP_011539128.1:p.Pro444=
XM_011540827.1:c.1036C=	XP_011539129.1:p.Pro346=
XM_011540828.1:c.1018C=	XP_011539130.1:p.Pro340=
XR_246241.1:n.1216C=
XR_246242.1:n.1200C=
NM_001319155.1:c.1216C=	NP_001306084.1:p.Pro406=
NM_001363587.1:c.1018C=	NP_001350516.1:p.Pro340=
NR_134988.1:n.1017C=
NR_134989.1:n.1208C=
NR_134990.1:n.1202C=
NR_134991.1:n.1189C=
NR_134992.1:n.818C=
NR_134993.1:n.952C=
NR_134994.1:n.1224C=
XM_017000465.1:c.1000C=	XP_016855954.1:p.Pro334=
XR_001737005.1:n.1290C=
NM_000778.4:c.1312C= MANE Select	NP_000769.2:p.Pro438=
NM_001319155.2:c.1216C=	NP_001306084.1:p.Pro406=
NM_001363587.2:c.1018C=	NP_001350516.1:p.Pro340=
NR_134988.2:n.1009C=
NR_134989.2:n.1200C=
NR_134990.2:n.1194C=
NR_134991.2:n.1181C=
NR_134992.2:n.810C=
NR_134993.2:n.944C=
NR_134994.2:n.1216C=