Canonical Allele Identifier: CA2474390760

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1681135486
• gnomAD v4: 1-46933136-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933136A>C , CM000663.2:g.46933136A>C	GRCh38
NC_000001.10:g.47398808A>C , CM000663.1:g.47398808A>C	GRCh37
NC_000001.9:g.47171395A>C	NCBI36
NG_007932.1:g.13349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1223-89T>G MANE Select	ENSP00000311095.4:n.1223-89T>G
ENST00000310638.8:c.1223-89T>G	ENSP00000311095.4:n.1223-89T>G
ENST00000371904.8:c.1226-89T>G	ENSP00000360971.4:n.1226-89T>G
ENST00000371905.1:c.1223-89T>G	ENSP00000360972.1:n.1223-89T>G
ENST00000462347.5:c.929-89T>G	ENSP00000477495.1:n.929-89T>G
ENST00000465874.5:c.*21-89T>G	ENSP00000476368.1:n.*21-89T>G
ENST00000468629.5:c.1127-299T>G	ENSP00000476619.1:n.1127-299T>G
ENST00000474458.5:c.743-299T>G	ENSP00000476988.1:n.743-299T>G
ENST00000475477.5:c.*82-299T>G	ENSP00000476854.1:n.*82-299T>G
NM_000778.3:c.1223-89T>G	NP_000769.2:n.1223-89T>G
XM_005270539.1:c.929-89T>G	XP_005270596.1:n.929-89T>G
XM_011540826.1:c.1241-89T>G	XP_011539128.1:n.1241-89T>G
XM_011540827.1:c.947-89T>G	XP_011539129.1:n.947-89T>G
XM_011540828.1:c.929-89T>G	XP_011539130.1:n.929-89T>G
XR_246241.1:n.1127-89T>G
XR_246242.1:n.1111-89T>G
NM_001319155.1:c.1127-89T>G	NP_001306084.1:n.1127-89T>G
NM_001363587.1:c.929-89T>G	NP_001350516.1:n.929-89T>G
NR_134988.1:n.928-89T>G
NR_134989.1:n.1119-89T>G
NR_134990.1:n.1178-299T>G
NR_134991.1:n.1100-89T>G
NR_134992.1:n.794-299T>G
NR_134993.1:n.928-299T>G
NR_134994.1:n.1135-89T>G
XM_017000465.1:c.911-89T>G	XP_016855954.1:n.911-89T>G
XR_001737005.1:n.1266-299T>G
NM_000778.4:c.1223-89T>G MANE Select	NP_000769.2:n.1223-89T>G
NM_001319155.2:c.1127-89T>G	NP_001306084.1:n.1127-89T>G
NM_001363587.2:c.929-89T>G	NP_001350516.1:n.929-89T>G
NR_134988.2:n.920-89T>G
NR_134989.2:n.1111-89T>G
NR_134990.2:n.1170-299T>G
NR_134991.2:n.1092-89T>G
NR_134992.2:n.786-299T>G
NR_134993.2:n.920-299T>G
NR_134994.2:n.1127-89T>G