Canonical Allele Identifier: CA21988135

Gene: CYP4A11

Linked Data

• dbSNP Id: rs569023065
• gnomAD v3: 1-46932620-G-A
• gnomAD v4: 1-46932620-G-A
• MyVariant Identifiers: chr1:g.47398292G>A (hg19) ; chr1:g.46932620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932620G>A , CM000663.2:g.46932620G>A	GRCh38
NC_000001.10:g.47398292G>A , CM000663.1:g.47398292G>A	GRCh37
NC_000001.9:g.47170879G>A	NCBI36
NG_007932.1:g.13865C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364+141C>T MANE Select	ENSP00000311095.4:n.1364+141C>T
ENST00000310638.8:c.1364+141C>T	ENSP00000311095.4:n.1364+141C>T
ENST00000371904.8:c.1367+141C>T	ENSP00000360971.4:n.1367+141C>T
ENST00000371905.1:c.*137C>T	ENSP00000360972.1:n.*137C>T
ENST00000462347.5:c.1070+141C>T	ENSP00000477495.1:n.1070+141C>T
ENST00000465874.5:c.*303C>T	ENSP00000476368.1:n.*303C>T
ENST00000468629.5:c.*69+141C>T	ENSP00000476619.1:n.*69+141C>T
ENST00000474458.5:c.*69+141C>T	ENSP00000476988.1:n.*69+141C>T
ENST00000475477.5:c.*158+141C>T	ENSP00000476854.1:n.*158+141C>T
NM_000778.3:c.1364+141C>T	NP_000769.2:n.1364+141C>T
XM_011540826.1:c.1382+141C>T	XP_011539128.1:n.1382+141C>T
XM_011540827.1:c.1088+141C>T	XP_011539129.1:n.1088+141C>T
XM_011540828.1:c.1070+141C>T	XP_011539130.1:n.1070+141C>T
XR_246241.1:n.1268+141C>T
XR_246242.1:n.1252+141C>T
NM_001319155.1:c.1268+141C>T	NP_001306084.1:n.1268+141C>T
NM_001363587.1:c.1070+141C>T	NP_001350516.1:n.1070+141C>T
NR_134988.1:n.1069+141C>T
NR_134989.1:n.1260+141C>T
NR_134990.1:n.1254+141C>T
NR_134991.1:n.1241+141C>T
NR_134992.1:n.870+141C>T
NR_134993.1:n.1004+141C>T
NR_134994.1:n.1276+141C>T
XM_017000465.1:c.1052+141C>T	XP_016855954.1:n.1052+141C>T
XR_001737005.1:n.1342+141C>T
NM_000778.4:c.1364+141C>T MANE Select	NP_000769.2:n.1364+141C>T
NM_001319155.2:c.1268+141C>T	NP_001306084.1:n.1268+141C>T
NM_001363587.2:c.1070+141C>T	NP_001350516.1:n.1070+141C>T
NR_134988.2:n.1061+141C>T
NR_134989.2:n.1252+141C>T
NR_134990.2:n.1246+141C>T
NR_134991.2:n.1233+141C>T
NR_134992.2:n.862+141C>T
NR_134993.2:n.996+141C>T
NR_134994.2:n.1268+141C>T