Canonical Allele Identifier: CA340223190

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398479A>C (hg19) ; chr1:g.46932807A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932807A>C , CM000663.2:g.46932807A>C	GRCh38
NC_000001.10:g.47398479A>C , CM000663.1:g.47398479A>C	GRCh37
NC_000001.9:g.47171066A>C	NCBI36
NG_007932.1:g.13678T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1318T>G MANE Select	ENSP00000311095.4:p.Ser440Ala
ENST00000310638.8:c.1318T>G	ENSP00000311095.4:p.Ser440Ala
ENST00000371904.8:c.1321T>G	ENSP00000360971.4:p.Ser441Ala
ENST00000371905.1:c.1318T>G	ENSP00000360972.1:p.Ser440Ala
ENST00000462347.5:c.1024T>G	ENSP00000477495.1:p.Ser342Ala
ENST00000465874.5:c.*116T>G	ENSP00000476368.1:n.*116T>G
ENST00000468629.5:c.*23T>G	ENSP00000476619.1:n.*23T>G
ENST00000474458.5:c.*23T>G	ENSP00000476988.1:n.*23T>G
ENST00000475477.5:c.*112T>G	ENSP00000476854.1:n.*112T>G
NM_000778.3:c.1318T>G	NP_000769.2:p.Ser440Ala
XM_005270539.1:c.1024T>G	XP_005270596.1:p.Ser342Ala
XM_011540826.1:c.1336T>G	XP_011539128.1:p.Ser446Ala
XM_011540827.1:c.1042T>G	XP_011539129.1:p.Ser348Ala
XM_011540828.1:c.1024T>G	XP_011539130.1:p.Ser342Ala
XR_246241.1:n.1222T>G
XR_246242.1:n.1206T>G
NM_001319155.1:c.1222T>G	NP_001306084.1:p.Ser408Ala
NM_001363587.1:c.1024T>G	NP_001350516.1:p.Ser342Ala
NR_134988.1:n.1023T>G
NR_134989.1:n.1214T>G
NR_134990.1:n.1208T>G
NR_134991.1:n.1195T>G
NR_134992.1:n.824T>G
NR_134993.1:n.958T>G
NR_134994.1:n.1230T>G
XM_017000465.1:c.1006T>G	XP_016855954.1:p.Ser336Ala
XR_001737005.1:n.1296T>G
NM_000778.4:c.1318T>G MANE Select	NP_000769.2:p.Ser440Ala
NM_001319155.2:c.1222T>G	NP_001306084.1:p.Ser408Ala
NM_001363587.2:c.1024T>G	NP_001350516.1:p.Ser342Ala
NR_134988.2:n.1015T>G
NR_134989.2:n.1206T>G
NR_134990.2:n.1200T>G
NR_134991.2:n.1187T>G
NR_134992.2:n.816T>G
NR_134993.2:n.950T>G
NR_134994.2:n.1222T>G