Canonical Allele Identifier: CA340223094

Gene: CYP4A11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364G>C MANE Select	ENSP00000311095.4:p.Arg455Thr
ENST00000310638.8:c.1364G>C	ENSP00000311095.4:p.Arg455Thr
ENST00000371904.8:c.1367G>C	ENSP00000360971.4:p.Arg456Thr
ENST00000371905.1:c.1364G>C	ENSP00000360972.1:p.Arg455Thr
ENST00000462347.5:c.1070G>C	ENSP00000477495.1:p.Arg357Thr
ENST00000465874.5:c.*162G>C	ENSP00000476368.1:n.*162G>C
ENST00000468629.5:c.*69G>C	ENSP00000476619.1:n.*69G>C
ENST00000474458.5:c.*69G>C	ENSP00000476988.1:n.*69G>C
ENST00000475477.5:c.*158G>C	ENSP00000476854.1:n.*158G>C
NM_000778.3:c.1364G>C	NP_000769.2:p.Arg455Thr
XM_005270539.1:c.1070G>C	XP_005270596.1:p.Arg357Thr
XM_011540826.1:c.1382G>C	XP_011539128.1:p.Arg461Thr
XM_011540827.1:c.1088G>C	XP_011539129.1:p.Arg363Thr
XM_011540828.1:c.1070G>C	XP_011539130.1:p.Arg357Thr
XR_246241.1:n.1268G>C
XR_246242.1:n.1252G>C
NM_001319155.1:c.1268G>C	NP_001306084.1:p.Arg423Thr
NM_001363587.1:c.1070G>C	NP_001350516.1:p.Arg357Thr
NR_134988.1:n.1069G>C
NR_134989.1:n.1260G>C
NR_134990.1:n.1254G>C
NR_134991.1:n.1241G>C
NR_134992.1:n.870G>C
NR_134993.1:n.1004G>C
NR_134994.1:n.1276G>C
XM_017000465.1:c.1052G>C	XP_016855954.1:p.Arg351Thr
XR_001737005.1:n.1342G>C
NM_000778.4:c.1364G>C MANE Select	NP_000769.2:p.Arg455Thr
NM_001319155.2:c.1268G>C	NP_001306084.1:p.Arg423Thr
NM_001363587.2:c.1070G>C	NP_001350516.1:p.Arg357Thr
NR_134988.2:n.1061G>C
NR_134989.2:n.1252G>C
NR_134990.2:n.1246G>C
NR_134991.2:n.1233G>C
NR_134992.2:n.862G>C
NR_134993.2:n.996G>C
NR_134994.2:n.1268G>C