Canonical Allele Identifier: CA340223171

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398469T>G (hg19) ; chr1:g.46932797T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932797T>G , CM000663.2:g.46932797T>G	GRCh38
NC_000001.10:g.47398469T>G , CM000663.1:g.47398469T>G	GRCh37
NC_000001.9:g.47171056T>G	NCBI36
NG_007932.1:g.13688A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1328A>C MANE Select	ENSP00000311095.4:p.His443Pro
ENST00000310638.8:c.1328A>C	ENSP00000311095.4:p.His443Pro
ENST00000371904.8:c.1331A>C	ENSP00000360971.4:p.His444Pro
ENST00000371905.1:c.1328A>C	ENSP00000360972.1:p.His443Pro
ENST00000462347.5:c.1034A>C	ENSP00000477495.1:p.His345Pro
ENST00000465874.5:c.*126A>C	ENSP00000476368.1:n.*126A>C
ENST00000468629.5:c.*33A>C	ENSP00000476619.1:n.*33A>C
ENST00000474458.5:c.*33A>C	ENSP00000476988.1:n.*33A>C
ENST00000475477.5:c.*122A>C	ENSP00000476854.1:n.*122A>C
NM_000778.3:c.1328A>C	NP_000769.2:p.His443Pro
XM_005270539.1:c.1034A>C	XP_005270596.1:p.His345Pro
XM_011540826.1:c.1346A>C	XP_011539128.1:p.His449Pro
XM_011540827.1:c.1052A>C	XP_011539129.1:p.His351Pro
XM_011540828.1:c.1034A>C	XP_011539130.1:p.His345Pro
XR_246241.1:n.1232A>C
XR_246242.1:n.1216A>C
NM_001319155.1:c.1232A>C	NP_001306084.1:p.His411Pro
NM_001363587.1:c.1034A>C	NP_001350516.1:p.His345Pro
NR_134988.1:n.1033A>C
NR_134989.1:n.1224A>C
NR_134990.1:n.1218A>C
NR_134991.1:n.1205A>C
NR_134992.1:n.834A>C
NR_134993.1:n.968A>C
NR_134994.1:n.1240A>C
XM_017000465.1:c.1016A>C	XP_016855954.1:p.His339Pro
XR_001737005.1:n.1306A>C
NM_000778.4:c.1328A>C MANE Select	NP_000769.2:p.His443Pro
NM_001319155.2:c.1232A>C	NP_001306084.1:p.His411Pro
NM_001363587.2:c.1034A>C	NP_001350516.1:p.His345Pro
NR_134988.2:n.1025A>C
NR_134989.2:n.1216A>C
NR_134990.2:n.1210A>C
NR_134991.2:n.1197A>C
NR_134992.2:n.826A>C
NR_134993.2:n.960A>C
NR_134994.2:n.1232A>C