Canonical Allele Identifier: CA736354948

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1412810851
• gnomAD v4: 1-46932369-G-T
• MyVariant Identifiers: chr1:g.47398041G>T (hg19) ; chr1:g.46932369G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932369G>T , CM000663.2:g.46932369G>T	GRCh38
NC_000001.10:g.47398041G>T , CM000663.1:g.47398041G>T	GRCh37
NC_000001.9:g.47170628G>T	NCBI36
NG_007932.1:g.14116C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1364+392C>A MANE Select	ENSP00000311095.4:n.1364+392C>A
ENST00000310638.8:c.1364+392C>A	ENSP00000311095.4:n.1364+392C>A
ENST00000371904.8:c.1367+392C>A	ENSP00000360971.4:n.1367+392C>A
ENST00000462347.5:c.1070+392C>A	ENSP00000477495.1:n.1070+392C>A
ENST00000465874.5:c.*554C>A	ENSP00000476368.1:n.*554C>A
ENST00000468629.5:c.*69+392C>A	ENSP00000476619.1:n.*69+392C>A
ENST00000474458.5:c.*69+392C>A	ENSP00000476988.1:n.*69+392C>A
ENST00000475477.5:c.*158+392C>A	ENSP00000476854.1:n.*158+392C>A
NM_000778.3:c.1364+392C>A	NP_000769.2:n.1364+392C>A
XM_011540826.1:c.1382+392C>A	XP_011539128.1:n.1382+392C>A
XM_011540827.1:c.1088+392C>A	XP_011539129.1:n.1088+392C>A
XM_011540828.1:c.1070+392C>A	XP_011539130.1:n.1070+392C>A
XR_246241.1:n.1268+392C>A
XR_246242.1:n.1252+392C>A
NM_001319155.1:c.1268+392C>A	NP_001306084.1:n.1268+392C>A
NM_001363587.1:c.1070+392C>A	NP_001350516.1:n.1070+392C>A
NR_134988.1:n.1069+392C>A
NR_134989.1:n.1260+392C>A
NR_134990.1:n.1254+392C>A
NR_134991.1:n.1241+392C>A
NR_134992.1:n.870+392C>A
NR_134993.1:n.1004+392C>A
NR_134994.1:n.1276+392C>A
XM_017000465.1:c.1052+392C>A	XP_016855954.1:n.1052+392C>A
XR_001737005.1:n.1342+392C>A
NM_000778.4:c.1364+392C>A MANE Select	NP_000769.2:n.1364+392C>A
NM_001319155.2:c.1268+392C>A	NP_001306084.1:n.1268+392C>A
NM_001363587.2:c.1070+392C>A	NP_001350516.1:n.1070+392C>A
NR_134988.2:n.1061+392C>A
NR_134989.2:n.1252+392C>A
NR_134990.2:n.1246+392C>A
NR_134991.2:n.1233+392C>A
NR_134992.2:n.862+392C>A
NR_134993.2:n.996+392C>A
NR_134994.2:n.1268+392C>A