Canonical Allele Identifier: CA2645486156

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932570-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932570G>T , CM000663.2:g.46932570G>T	GRCh38
NC_000001.10:g.47398242G>T , CM000663.1:g.47398242G>T	GRCh37
NC_000001.9:g.47170829G>T	NCBI36
NG_007932.1:g.13915C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1364+191C>A MANE Select	ENSP00000311095.4:n.1364+191C>A
ENST00000310638.8:c.1364+191C>A	ENSP00000311095.4:n.1364+191C>A
ENST00000371904.8:c.1367+191C>A	ENSP00000360971.4:n.1367+191C>A
ENST00000371905.1:c.*187C>A	ENSP00000360972.1:n.*187C>A
ENST00000462347.5:c.1070+191C>A	ENSP00000477495.1:n.1070+191C>A
ENST00000465874.5:c.*353C>A	ENSP00000476368.1:n.*353C>A
ENST00000468629.5:c.*69+191C>A	ENSP00000476619.1:n.*69+191C>A
ENST00000474458.5:c.*69+191C>A	ENSP00000476988.1:n.*69+191C>A
ENST00000475477.5:c.*158+191C>A	ENSP00000476854.1:n.*158+191C>A
NM_000778.3:c.1364+191C>A	NP_000769.2:n.1364+191C>A
XM_011540826.1:c.1382+191C>A	XP_011539128.1:n.1382+191C>A
XM_011540827.1:c.1088+191C>A	XP_011539129.1:n.1088+191C>A
XM_011540828.1:c.1070+191C>A	XP_011539130.1:n.1070+191C>A
XR_246241.1:n.1268+191C>A
XR_246242.1:n.1252+191C>A
NM_001319155.1:c.1268+191C>A	NP_001306084.1:n.1268+191C>A
NM_001363587.1:c.1070+191C>A	NP_001350516.1:n.1070+191C>A
NR_134988.1:n.1069+191C>A
NR_134989.1:n.1260+191C>A
NR_134990.1:n.1254+191C>A
NR_134991.1:n.1241+191C>A
NR_134992.1:n.870+191C>A
NR_134993.1:n.1004+191C>A
NR_134994.1:n.1276+191C>A
XM_017000465.1:c.1052+191C>A	XP_016855954.1:n.1052+191C>A
XR_001737005.1:n.1342+191C>A
NM_000778.4:c.1364+191C>A MANE Select	NP_000769.2:n.1364+191C>A
NM_001319155.2:c.1268+191C>A	NP_001306084.1:n.1268+191C>A
NM_001363587.2:c.1070+191C>A	NP_001350516.1:n.1070+191C>A
NR_134988.2:n.1061+191C>A
NR_134989.2:n.1252+191C>A
NR_134990.2:n.1246+191C>A
NR_134991.2:n.1233+191C>A
NR_134992.2:n.862+191C>A
NR_134993.2:n.996+191C>A
NR_134994.2:n.1268+191C>A