Canonical Allele Identifier: CA340223191

Gene: CYP4A11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1318T>C MANE Select	ENSP00000311095.4:p.Ser440Pro
ENST00000310638.8:c.1318T>C	ENSP00000311095.4:p.Ser440Pro
ENST00000371904.8:c.1321T>C	ENSP00000360971.4:p.Ser441Pro
ENST00000371905.1:c.1318T>C	ENSP00000360972.1:p.Ser440Pro
ENST00000462347.5:c.1024T>C	ENSP00000477495.1:p.Ser342Pro
ENST00000465874.5:c.*116T>C	ENSP00000476368.1:n.*116T>C
ENST00000468629.5:c.*23T>C	ENSP00000476619.1:n.*23T>C
ENST00000474458.5:c.*23T>C	ENSP00000476988.1:n.*23T>C
ENST00000475477.5:c.*112T>C	ENSP00000476854.1:n.*112T>C
NM_000778.3:c.1318T>C	NP_000769.2:p.Ser440Pro
XM_005270539.1:c.1024T>C	XP_005270596.1:p.Ser342Pro
XM_011540826.1:c.1336T>C	XP_011539128.1:p.Ser446Pro
XM_011540827.1:c.1042T>C	XP_011539129.1:p.Ser348Pro
XM_011540828.1:c.1024T>C	XP_011539130.1:p.Ser342Pro
XR_246241.1:n.1222T>C
XR_246242.1:n.1206T>C
NM_001319155.1:c.1222T>C	NP_001306084.1:p.Ser408Pro
NM_001363587.1:c.1024T>C	NP_001350516.1:p.Ser342Pro
NR_134988.1:n.1023T>C
NR_134989.1:n.1214T>C
NR_134990.1:n.1208T>C
NR_134991.1:n.1195T>C
NR_134992.1:n.824T>C
NR_134993.1:n.958T>C
NR_134994.1:n.1230T>C
XM_017000465.1:c.1006T>C	XP_016855954.1:p.Ser336Pro
XR_001737005.1:n.1296T>C
NM_000778.4:c.1318T>C MANE Select	NP_000769.2:p.Ser440Pro
NM_001319155.2:c.1222T>C	NP_001306084.1:p.Ser408Pro
NM_001363587.2:c.1024T>C	NP_001350516.1:p.Ser342Pro
NR_134988.2:n.1015T>C
NR_134989.2:n.1206T>C
NR_134990.2:n.1200T>C
NR_134991.2:n.1187T>C
NR_134992.2:n.816T>C
NR_134993.2:n.950T>C
NR_134994.2:n.1222T>C