Canonical Allele Identifier: CA340223095

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398433C>T (hg19) ; chr1:g.46932761C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932761C>T , CM000663.2:g.46932761C>T	GRCh38
NC_000001.10:g.47398433C>T , CM000663.1:g.47398433C>T	GRCh37
NC_000001.9:g.47171020C>T	NCBI36
NG_007932.1:g.13724G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364G>A MANE Select	ENSP00000311095.4:p.Arg455Lys
ENST00000310638.8:c.1364G>A	ENSP00000311095.4:p.Arg455Lys
ENST00000371904.8:c.1367G>A	ENSP00000360971.4:p.Arg456Lys
ENST00000371905.1:c.1364G>A	ENSP00000360972.1:p.Arg455Lys
ENST00000462347.5:c.1070G>A	ENSP00000477495.1:p.Arg357Lys
ENST00000465874.5:c.*162G>A	ENSP00000476368.1:n.*162G>A
ENST00000468629.5:c.*69G>A	ENSP00000476619.1:n.*69G>A
ENST00000474458.5:c.*69G>A	ENSP00000476988.1:n.*69G>A
ENST00000475477.5:c.*158G>A	ENSP00000476854.1:n.*158G>A
NM_000778.3:c.1364G>A	NP_000769.2:p.Arg455Lys
XM_005270539.1:c.1070G>A	XP_005270596.1:p.Arg357Lys
XM_011540826.1:c.1382G>A	XP_011539128.1:p.Arg461Lys
XM_011540827.1:c.1088G>A	XP_011539129.1:p.Arg363Lys
XM_011540828.1:c.1070G>A	XP_011539130.1:p.Arg357Lys
XR_246241.1:n.1268G>A
XR_246242.1:n.1252G>A
NM_001319155.1:c.1268G>A	NP_001306084.1:p.Arg423Lys
NM_001363587.1:c.1070G>A	NP_001350516.1:p.Arg357Lys
NR_134988.1:n.1069G>A
NR_134989.1:n.1260G>A
NR_134990.1:n.1254G>A
NR_134991.1:n.1241G>A
NR_134992.1:n.870G>A
NR_134993.1:n.1004G>A
NR_134994.1:n.1276G>A
XM_017000465.1:c.1052G>A	XP_016855954.1:p.Arg351Lys
XR_001737005.1:n.1342G>A
NM_000778.4:c.1364G>A MANE Select	NP_000769.2:p.Arg455Lys
NM_001319155.2:c.1268G>A	NP_001306084.1:p.Arg423Lys
NM_001363587.2:c.1070G>A	NP_001350516.1:p.Arg357Lys
NR_134988.2:n.1061G>A
NR_134989.2:n.1252G>A
NR_134990.2:n.1246G>A
NR_134991.2:n.1233G>A
NR_134992.2:n.862G>A
NR_134993.2:n.996G>A
NR_134994.2:n.1268G>A