Canonical Allele Identifier: CA340223270

Gene: CYP4A11

Linked Data

• gnomAD v4: 1-46932987-G-T
• MyVariant Identifiers: chr1:g.47398659G>T (hg19) ; chr1:g.46932987G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932987G>T , CM000663.2:g.46932987G>T	GRCh38
NC_000001.10:g.47398659G>T , CM000663.1:g.47398659G>T	GRCh37
NC_000001.9:g.47171246G>T	NCBI36
NG_007932.1:g.13498C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1283C>A MANE Select	ENSP00000311095.4:p.Pro428Gln
ENST00000310638.8:c.1283C>A	ENSP00000311095.4:p.Pro428Gln
ENST00000371904.8:c.1286C>A	ENSP00000360971.4:p.Pro429Gln
ENST00000371905.1:c.1283C>A	ENSP00000360972.1:p.Pro428Gln
ENST00000462347.5:c.989C>A	ENSP00000477495.1:p.Pro330Gln
ENST00000465874.5:c.*81C>A	ENSP00000476368.1:n.*81C>A
ENST00000468629.5:c.1127-150C>A	ENSP00000476619.1:n.1127-150C>A
ENST00000474458.5:c.743-150C>A	ENSP00000476988.1:n.743-150C>A
ENST00000475477.5:c.*82-150C>A	ENSP00000476854.1:n.*82-150C>A
NM_000778.3:c.1283C>A	NP_000769.2:p.Pro428Gln
XM_005270539.1:c.989C>A	XP_005270596.1:p.Pro330Gln
XM_011540826.1:c.1301C>A	XP_011539128.1:p.Pro434Gln
XM_011540827.1:c.1007C>A	XP_011539129.1:p.Pro336Gln
XM_011540828.1:c.989C>A	XP_011539130.1:p.Pro330Gln
XR_246241.1:n.1187C>A
XR_246242.1:n.1171C>A
NM_001319155.1:c.1187C>A	NP_001306084.1:p.Pro396Gln
NM_001363587.1:c.989C>A	NP_001350516.1:p.Pro330Gln
NR_134988.1:n.988C>A
NR_134989.1:n.1179C>A
NR_134990.1:n.1178-150C>A
NR_134991.1:n.1160C>A
NR_134992.1:n.794-150C>A
NR_134993.1:n.928-150C>A
NR_134994.1:n.1195C>A
XM_017000465.1:c.971C>A	XP_016855954.1:p.Pro324Gln
XR_001737005.1:n.1266-150C>A
NM_000778.4:c.1283C>A MANE Select	NP_000769.2:p.Pro428Gln
NM_001319155.2:c.1187C>A	NP_001306084.1:p.Pro396Gln
NM_001363587.2:c.989C>A	NP_001350516.1:p.Pro330Gln
NR_134988.2:n.980C>A
NR_134989.2:n.1171C>A
NR_134990.2:n.1170-150C>A
NR_134991.2:n.1152C>A
NR_134992.2:n.786-150C>A
NR_134993.2:n.920-150C>A
NR_134994.2:n.1187C>A