Canonical Allele Identifier: CA340223104

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398439C>G (hg19) ; chr1:g.46932767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932767C>G , CM000663.2:g.46932767C>G	GRCh38
NC_000001.10:g.47398439C>G , CM000663.1:g.47398439C>G	GRCh37
NC_000001.9:g.47171026C>G	NCBI36
NG_007932.1:g.13718G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1358G>C MANE Select	ENSP00000311095.4:p.Gly453Ala
ENST00000310638.8:c.1358G>C	ENSP00000311095.4:p.Gly453Ala
ENST00000371904.8:c.1361G>C	ENSP00000360971.4:p.Gly454Ala
ENST00000371905.1:c.1358G>C	ENSP00000360972.1:p.Gly453Ala
ENST00000462347.5:c.1064G>C	ENSP00000477495.1:p.Gly355Ala
ENST00000465874.5:c.*156G>C	ENSP00000476368.1:n.*156G>C
ENST00000468629.5:c.*63G>C	ENSP00000476619.1:n.*63G>C
ENST00000474458.5:c.*63G>C	ENSP00000476988.1:n.*63G>C
ENST00000475477.5:c.*152G>C	ENSP00000476854.1:n.*152G>C
NM_000778.3:c.1358G>C	NP_000769.2:p.Gly453Ala
XM_005270539.1:c.1064G>C	XP_005270596.1:p.Gly355Ala
XM_011540826.1:c.1376G>C	XP_011539128.1:p.Gly459Ala
XM_011540827.1:c.1082G>C	XP_011539129.1:p.Gly361Ala
XM_011540828.1:c.1064G>C	XP_011539130.1:p.Gly355Ala
XR_246241.1:n.1262G>C
XR_246242.1:n.1246G>C
NM_001319155.1:c.1262G>C	NP_001306084.1:p.Gly421Ala
NM_001363587.1:c.1064G>C	NP_001350516.1:p.Gly355Ala
NR_134988.1:n.1063G>C
NR_134989.1:n.1254G>C
NR_134990.1:n.1248G>C
NR_134991.1:n.1235G>C
NR_134992.1:n.864G>C
NR_134993.1:n.998G>C
NR_134994.1:n.1270G>C
XM_017000465.1:c.1046G>C	XP_016855954.1:p.Gly349Ala
XR_001737005.1:n.1336G>C
NM_000778.4:c.1358G>C MANE Select	NP_000769.2:p.Gly453Ala
NM_001319155.2:c.1262G>C	NP_001306084.1:p.Gly421Ala
NM_001363587.2:c.1064G>C	NP_001350516.1:p.Gly355Ala
NR_134988.2:n.1055G>C
NR_134989.2:n.1246G>C
NR_134990.2:n.1240G>C
NR_134991.2:n.1227G>C
NR_134992.2:n.856G>C
NR_134993.2:n.990G>C
NR_134994.2:n.1262G>C