Canonical Allele Identifier: CA340223254

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398510C>A (hg19) ; chr1:g.46932838C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932838C>A , CM000663.2:g.46932838C>A	GRCh38
NC_000001.10:g.47398510C>A , CM000663.1:g.47398510C>A	GRCh37
NC_000001.9:g.47171097C>A	NCBI36
NG_007932.1:g.13647G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1288-1G>T MANE Select	ENSP00000311095.4:n.1288-1G>T
ENST00000310638.8:c.1288-1G>T	ENSP00000311095.4:n.1288-1G>T
ENST00000371904.8:c.1291-1G>T	ENSP00000360971.4:n.1291-1G>T
ENST00000371905.1:c.1288-1G>T	ENSP00000360972.1:n.1288-1G>T
ENST00000462347.5:c.994-1G>T	ENSP00000477495.1:n.994-1G>T
ENST00000465874.5:c.*86-1G>T	ENSP00000476368.1:n.*86-1G>T
ENST00000468629.5:c.1127-1G>T	ENSP00000476619.1:n.1127-1G>T
ENST00000474458.5:c.743-1G>T	ENSP00000476988.1:n.743-1G>T
ENST00000475477.5:c.*82-1G>T	ENSP00000476854.1:n.*82-1G>T
NM_000778.3:c.1288-1G>T	NP_000769.2:n.1288-1G>T
XM_005270539.1:c.994-1G>T	XP_005270596.1:n.994-1G>T
XM_011540826.1:c.1306-1G>T	XP_011539128.1:n.1306-1G>T
XM_011540827.1:c.1012-1G>T	XP_011539129.1:n.1012-1G>T
XM_011540828.1:c.994-1G>T	XP_011539130.1:n.994-1G>T
XR_246241.1:n.1192-1G>T
XR_246242.1:n.1176-1G>T
NM_001319155.1:c.1192-1G>T	NP_001306084.1:n.1192-1G>T
NM_001363587.1:c.994-1G>T	NP_001350516.1:n.994-1G>T
NR_134988.1:n.993-1G>T
NR_134989.1:n.1184-1G>T
NR_134990.1:n.1178-1G>T
NR_134991.1:n.1165-1G>T
NR_134992.1:n.794-1G>T
NR_134993.1:n.928-1G>T
NR_134994.1:n.1200-1G>T
XM_017000465.1:c.976-1G>T	XP_016855954.1:n.976-1G>T
XR_001737005.1:n.1266-1G>T
NM_000778.4:c.1288-1G>T MANE Select	NP_000769.2:n.1288-1G>T
NM_001319155.2:c.1192-1G>T	NP_001306084.1:n.1192-1G>T
NM_001363587.2:c.994-1G>T	NP_001350516.1:n.994-1G>T
NR_134988.2:n.985-1G>T
NR_134989.2:n.1176-1G>T
NR_134990.2:n.1170-1G>T
NR_134991.2:n.1157-1G>T
NR_134992.2:n.786-1G>T
NR_134993.2:n.920-1G>T
NR_134994.2:n.1192-1G>T