Canonical Allele Identifier: CA340223106

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398440C>G (hg19) ; chr1:g.46932768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932768C>G , CM000663.2:g.46932768C>G	GRCh38
NC_000001.10:g.47398440C>G , CM000663.1:g.47398440C>G	GRCh37
NC_000001.9:g.47171027C>G	NCBI36
NG_007932.1:g.13717G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1357G>C MANE Select	ENSP00000311095.4:p.Gly453Arg
ENST00000310638.8:c.1357G>C	ENSP00000311095.4:p.Gly453Arg
ENST00000371904.8:c.1360G>C	ENSP00000360971.4:p.Gly454Arg
ENST00000371905.1:c.1357G>C	ENSP00000360972.1:p.Gly453Arg
ENST00000462347.5:c.1063G>C	ENSP00000477495.1:p.Gly355Arg
ENST00000465874.5:c.*155G>C	ENSP00000476368.1:n.*155G>C
ENST00000468629.5:c.*62G>C	ENSP00000476619.1:n.*62G>C
ENST00000474458.5:c.*62G>C	ENSP00000476988.1:n.*62G>C
ENST00000475477.5:c.*151G>C	ENSP00000476854.1:n.*151G>C
NM_000778.3:c.1357G>C	NP_000769.2:p.Gly453Arg
XM_005270539.1:c.1063G>C	XP_005270596.1:p.Gly355Arg
XM_011540826.1:c.1375G>C	XP_011539128.1:p.Gly459Arg
XM_011540827.1:c.1081G>C	XP_011539129.1:p.Gly361Arg
XM_011540828.1:c.1063G>C	XP_011539130.1:p.Gly355Arg
XR_246241.1:n.1261G>C
XR_246242.1:n.1245G>C
NM_001319155.1:c.1261G>C	NP_001306084.1:p.Gly421Arg
NM_001363587.1:c.1063G>C	NP_001350516.1:p.Gly355Arg
NR_134988.1:n.1062G>C
NR_134989.1:n.1253G>C
NR_134990.1:n.1247G>C
NR_134991.1:n.1234G>C
NR_134992.1:n.863G>C
NR_134993.1:n.997G>C
NR_134994.1:n.1269G>C
XM_017000465.1:c.1045G>C	XP_016855954.1:p.Gly349Arg
XR_001737005.1:n.1335G>C
NM_000778.4:c.1357G>C MANE Select	NP_000769.2:p.Gly453Arg
NM_001319155.2:c.1261G>C	NP_001306084.1:p.Gly421Arg
NM_001363587.2:c.1063G>C	NP_001350516.1:p.Gly355Arg
NR_134988.2:n.1054G>C
NR_134989.2:n.1245G>C
NR_134990.2:n.1239G>C
NR_134991.2:n.1226G>C
NR_134992.2:n.855G>C
NR_134993.2:n.989G>C
NR_134994.2:n.1261G>C