Canonical Allele Identifier: CA340223289

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398668C>A (hg19) ; chr1:g.46932996C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932996C>A , CM000663.2:g.46932996C>A	GRCh38
NC_000001.10:g.47398668C>A , CM000663.1:g.47398668C>A	GRCh37
NC_000001.9:g.47171255C>A	NCBI36
NG_007932.1:g.13489G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1274G>T MANE Select	ENSP00000311095.4:p.Trp425Leu
ENST00000310638.8:c.1274G>T	ENSP00000311095.4:p.Trp425Leu
ENST00000371904.8:c.1277G>T	ENSP00000360971.4:p.Trp426Leu
ENST00000371905.1:c.1274G>T	ENSP00000360972.1:p.Trp425Leu
ENST00000462347.5:c.980G>T	ENSP00000477495.1:p.Trp327Leu
ENST00000465874.5:c.*72G>T	ENSP00000476368.1:n.*72G>T
ENST00000468629.5:c.1127-159G>T	ENSP00000476619.1:n.1127-159G>T
ENST00000474458.5:c.743-159G>T	ENSP00000476988.1:n.743-159G>T
ENST00000475477.5:c.*82-159G>T	ENSP00000476854.1:n.*82-159G>T
NM_000778.3:c.1274G>T	NP_000769.2:p.Trp425Leu
XM_005270539.1:c.980G>T	XP_005270596.1:p.Trp327Leu
XM_011540826.1:c.1292G>T	XP_011539128.1:p.Trp431Leu
XM_011540827.1:c.998G>T	XP_011539129.1:p.Trp333Leu
XM_011540828.1:c.980G>T	XP_011539130.1:p.Trp327Leu
XR_246241.1:n.1178G>T
XR_246242.1:n.1162G>T
NM_001319155.1:c.1178G>T	NP_001306084.1:p.Trp393Leu
NM_001363587.1:c.980G>T	NP_001350516.1:p.Trp327Leu
NR_134988.1:n.979G>T
NR_134989.1:n.1170G>T
NR_134990.1:n.1178-159G>T
NR_134991.1:n.1151G>T
NR_134992.1:n.794-159G>T
NR_134993.1:n.928-159G>T
NR_134994.1:n.1186G>T
XM_017000465.1:c.962G>T	XP_016855954.1:p.Trp321Leu
XR_001737005.1:n.1266-159G>T
NM_000778.4:c.1274G>T MANE Select	NP_000769.2:p.Trp425Leu
NM_001319155.2:c.1178G>T	NP_001306084.1:p.Trp393Leu
NM_001363587.2:c.980G>T	NP_001350516.1:p.Trp327Leu
NR_134988.2:n.971G>T
NR_134989.2:n.1162G>T
NR_134990.2:n.1170-159G>T
NR_134991.2:n.1143G>T
NR_134992.2:n.786-159G>T
NR_134993.2:n.920-159G>T
NR_134994.2:n.1178G>T