Canonical Allele Identifier: CA340223119

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398446A>T (hg19) ; chr1:g.46932774A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932774A>T , CM000663.2:g.46932774A>T	GRCh38
NC_000001.10:g.47398446A>T , CM000663.1:g.47398446A>T	GRCh37
NC_000001.9:g.47171033A>T	NCBI36
NG_007932.1:g.13711T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1351T>A MANE Select	ENSP00000311095.4:p.Ser451Thr
ENST00000310638.8:c.1351T>A	ENSP00000311095.4:p.Ser451Thr
ENST00000371904.8:c.1354T>A	ENSP00000360971.4:p.Ser452Thr
ENST00000371905.1:c.1351T>A	ENSP00000360972.1:p.Ser451Thr
ENST00000462347.5:c.1057T>A	ENSP00000477495.1:p.Ser353Thr
ENST00000465874.5:c.*149T>A	ENSP00000476368.1:n.*149T>A
ENST00000468629.5:c.*56T>A	ENSP00000476619.1:n.*56T>A
ENST00000474458.5:c.*56T>A	ENSP00000476988.1:n.*56T>A
ENST00000475477.5:c.*145T>A	ENSP00000476854.1:n.*145T>A
NM_000778.3:c.1351T>A	NP_000769.2:p.Ser451Thr
XM_005270539.1:c.1057T>A	XP_005270596.1:p.Ser353Thr
XM_011540826.1:c.1369T>A	XP_011539128.1:p.Ser457Thr
XM_011540827.1:c.1075T>A	XP_011539129.1:p.Ser359Thr
XM_011540828.1:c.1057T>A	XP_011539130.1:p.Ser353Thr
XR_246241.1:n.1255T>A
XR_246242.1:n.1239T>A
NM_001319155.1:c.1255T>A	NP_001306084.1:p.Ser419Thr
NM_001363587.1:c.1057T>A	NP_001350516.1:p.Ser353Thr
NR_134988.1:n.1056T>A
NR_134989.1:n.1247T>A
NR_134990.1:n.1241T>A
NR_134991.1:n.1228T>A
NR_134992.1:n.857T>A
NR_134993.1:n.991T>A
NR_134994.1:n.1263T>A
XM_017000465.1:c.1039T>A	XP_016855954.1:p.Ser347Thr
XR_001737005.1:n.1329T>A
NM_000778.4:c.1351T>A MANE Select	NP_000769.2:p.Ser451Thr
NM_001319155.2:c.1255T>A	NP_001306084.1:p.Ser419Thr
NM_001363587.2:c.1057T>A	NP_001350516.1:p.Ser353Thr
NR_134988.2:n.1048T>A
NR_134989.2:n.1239T>A
NR_134990.2:n.1233T>A
NR_134991.2:n.1220T>A
NR_134992.2:n.849T>A
NR_134993.2:n.983T>A
NR_134994.2:n.1255T>A