Canonical Allele Identifier: CA340223195

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398482C>A (hg19) ; chr1:g.46932810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932810C>A , CM000663.2:g.46932810C>A	GRCh38
NC_000001.10:g.47398482C>A , CM000663.1:g.47398482C>A	GRCh37
NC_000001.9:g.47171069C>A	NCBI36
NG_007932.1:g.13675G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1315G>T MANE Select	ENSP00000311095.4:p.Gly439Cys
ENST00000310638.8:c.1315G>T	ENSP00000311095.4:p.Gly439Cys
ENST00000371904.8:c.1318G>T	ENSP00000360971.4:p.Gly440Cys
ENST00000371905.1:c.1315G>T	ENSP00000360972.1:p.Gly439Cys
ENST00000462347.5:c.1021G>T	ENSP00000477495.1:p.Gly341Cys
ENST00000465874.5:c.*113G>T	ENSP00000476368.1:n.*113G>T
ENST00000468629.5:c.*20G>T	ENSP00000476619.1:n.*20G>T
ENST00000474458.5:c.*20G>T	ENSP00000476988.1:n.*20G>T
ENST00000475477.5:c.*109G>T	ENSP00000476854.1:n.*109G>T
NM_000778.3:c.1315G>T	NP_000769.2:p.Gly439Cys
XM_005270539.1:c.1021G>T	XP_005270596.1:p.Gly341Cys
XM_011540826.1:c.1333G>T	XP_011539128.1:p.Gly445Cys
XM_011540827.1:c.1039G>T	XP_011539129.1:p.Gly347Cys
XM_011540828.1:c.1021G>T	XP_011539130.1:p.Gly341Cys
XR_246241.1:n.1219G>T
XR_246242.1:n.1203G>T
NM_001319155.1:c.1219G>T	NP_001306084.1:p.Gly407Cys
NM_001363587.1:c.1021G>T	NP_001350516.1:p.Gly341Cys
NR_134988.1:n.1020G>T
NR_134989.1:n.1211G>T
NR_134990.1:n.1205G>T
NR_134991.1:n.1192G>T
NR_134992.1:n.821G>T
NR_134993.1:n.955G>T
NR_134994.1:n.1227G>T
XM_017000465.1:c.1003G>T	XP_016855954.1:p.Gly335Cys
XR_001737005.1:n.1293G>T
NM_000778.4:c.1315G>T MANE Select	NP_000769.2:p.Gly439Cys
NM_001319155.2:c.1219G>T	NP_001306084.1:p.Gly407Cys
NM_001363587.2:c.1021G>T	NP_001350516.1:p.Gly341Cys
NR_134988.2:n.1012G>T
NR_134989.2:n.1203G>T
NR_134990.2:n.1197G>T
NR_134991.2:n.1184G>T
NR_134992.2:n.813G>T
NR_134993.2:n.947G>T
NR_134994.2:n.1219G>T