Canonical Allele Identifier: CA340223164

Gene: CYP4A11

Linked Data

• COSMIC: COSM4422456
• MyVariant Identifiers: chr1:g.47398467T>A (hg19) ; chr1:g.46932795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932795T>A , CM000663.2:g.46932795T>A	GRCh38
NC_000001.10:g.47398467T>A , CM000663.1:g.47398467T>A	GRCh37
NC_000001.9:g.47171054T>A	NCBI36
NG_007932.1:g.13690A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1330A>T MANE Select	ENSP00000311095.4:p.Ser444Cys
ENST00000310638.8:c.1330A>T	ENSP00000311095.4:p.Ser444Cys
ENST00000371904.8:c.1333A>T	ENSP00000360971.4:p.Ser445Cys
ENST00000371905.1:c.1330A>T	ENSP00000360972.1:p.Ser444Cys
ENST00000462347.5:c.1036A>T	ENSP00000477495.1:p.Ser346Cys
ENST00000465874.5:c.*128A>T	ENSP00000476368.1:n.*128A>T
ENST00000468629.5:c.*35A>T	ENSP00000476619.1:n.*35A>T
ENST00000474458.5:c.*35A>T	ENSP00000476988.1:n.*35A>T
ENST00000475477.5:c.*124A>T	ENSP00000476854.1:n.*124A>T
NM_000778.3:c.1330A>T	NP_000769.2:p.Ser444Cys
XM_005270539.1:c.1036A>T	XP_005270596.1:p.Ser346Cys
XM_011540826.1:c.1348A>T	XP_011539128.1:p.Ser450Cys
XM_011540827.1:c.1054A>T	XP_011539129.1:p.Ser352Cys
XM_011540828.1:c.1036A>T	XP_011539130.1:p.Ser346Cys
XR_246241.1:n.1234A>T
XR_246242.1:n.1218A>T
NM_001319155.1:c.1234A>T	NP_001306084.1:p.Ser412Cys
NM_001363587.1:c.1036A>T	NP_001350516.1:p.Ser346Cys
NR_134988.1:n.1035A>T
NR_134989.1:n.1226A>T
NR_134990.1:n.1220A>T
NR_134991.1:n.1207A>T
NR_134992.1:n.836A>T
NR_134993.1:n.970A>T
NR_134994.1:n.1242A>T
XM_017000465.1:c.1018A>T	XP_016855954.1:p.Ser340Cys
XR_001737005.1:n.1308A>T
NM_000778.4:c.1330A>T MANE Select	NP_000769.2:p.Ser444Cys
NM_001319155.2:c.1234A>T	NP_001306084.1:p.Ser412Cys
NM_001363587.2:c.1036A>T	NP_001350516.1:p.Ser346Cys
NR_134988.2:n.1027A>T
NR_134989.2:n.1218A>T
NR_134990.2:n.1212A>T
NR_134991.2:n.1199A>T
NR_134992.2:n.828A>T
NR_134993.2:n.962A>T
NR_134994.2:n.1234A>T