Canonical Allele Identifier: CA340223370

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398707A>C (hg19) ; chr1:g.46933035A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933035A>C , CM000663.2:g.46933035A>C	GRCh38
NC_000001.10:g.47398707A>C , CM000663.1:g.47398707A>C	GRCh37
NC_000001.9:g.47171294A>C	NCBI36
NG_007932.1:g.13450T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1235T>G MANE Select	ENSP00000311095.4:p.Leu412Arg
ENST00000310638.8:c.1235T>G	ENSP00000311095.4:p.Leu412Arg
ENST00000371904.8:c.1238T>G	ENSP00000360971.4:p.Leu413Arg
ENST00000371905.1:c.1235T>G	ENSP00000360972.1:p.Leu412Arg
ENST00000462347.5:c.941T>G	ENSP00000477495.1:p.Leu314Arg
ENST00000465874.5:c.*33T>G	ENSP00000476368.1:n.*33T>G
ENST00000468629.5:c.1127-198T>G	ENSP00000476619.1:n.1127-198T>G
ENST00000474458.5:c.743-198T>G	ENSP00000476988.1:n.743-198T>G
ENST00000475477.5:c.*82-198T>G	ENSP00000476854.1:n.*82-198T>G
NM_000778.3:c.1235T>G	NP_000769.2:p.Leu412Arg
XM_005270539.1:c.941T>G	XP_005270596.1:p.Leu314Arg
XM_011540826.1:c.1253T>G	XP_011539128.1:p.Leu418Arg
XM_011540827.1:c.959T>G	XP_011539129.1:p.Leu320Arg
XM_011540828.1:c.941T>G	XP_011539130.1:p.Leu314Arg
XR_246241.1:n.1139T>G
XR_246242.1:n.1123T>G
NM_001319155.1:c.1139T>G	NP_001306084.1:p.Leu380Arg
NM_001363587.1:c.941T>G	NP_001350516.1:p.Leu314Arg
NR_134988.1:n.940T>G
NR_134989.1:n.1131T>G
NR_134990.1:n.1178-198T>G
NR_134991.1:n.1112T>G
NR_134992.1:n.794-198T>G
NR_134993.1:n.928-198T>G
NR_134994.1:n.1147T>G
XM_017000465.1:c.923T>G	XP_016855954.1:p.Leu308Arg
XR_001737005.1:n.1266-198T>G
NM_000778.4:c.1235T>G MANE Select	NP_000769.2:p.Leu412Arg
NM_001319155.2:c.1139T>G	NP_001306084.1:p.Leu380Arg
NM_001363587.2:c.941T>G	NP_001350516.1:p.Leu314Arg
NR_134988.2:n.932T>G
NR_134989.2:n.1123T>G
NR_134990.2:n.1170-198T>G
NR_134991.2:n.1104T>G
NR_134992.2:n.786-198T>G
NR_134993.2:n.920-198T>G
NR_134994.2:n.1139T>G