Canonical Allele Identifier: CA340223381

Gene: CYP4A11

Linked Data

• dbSNP Id: rs777439629
• MyVariant Identifiers: chr1:g.47398712C>T (hg19) ; chr1:g.46933040C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933040C>T , CM000663.2:g.46933040C>T	GRCh38
NC_000001.10:g.47398712C>T , CM000663.1:g.47398712C>T	GRCh37
NC_000001.9:g.47171299C>T	NCBI36
NG_007932.1:g.13445G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1230G>A MANE Select	ENSP00000311095.4:p.Met410Ile
ENST00000310638.8:c.1230G>A	ENSP00000311095.4:p.Met410Ile
ENST00000371904.8:c.1233G>A	ENSP00000360971.4:p.Met411Ile
ENST00000371905.1:c.1230G>A	ENSP00000360972.1:p.Met410Ile
ENST00000462347.5:c.936G>A	ENSP00000477495.1:p.Met312Ile
ENST00000465874.5:c.*28G>A	ENSP00000476368.1:n.*28G>A
ENST00000468629.5:c.1127-203G>A	ENSP00000476619.1:n.1127-203G>A
ENST00000474458.5:c.743-203G>A	ENSP00000476988.1:n.743-203G>A
ENST00000475477.5:c.*82-203G>A	ENSP00000476854.1:n.*82-203G>A
NM_000778.3:c.1230G>A	NP_000769.2:p.Met410Ile
XM_005270539.1:c.936G>A	XP_005270596.1:p.Met312Ile
XM_011540826.1:c.1248G>A	XP_011539128.1:p.Met416Ile
XM_011540827.1:c.954G>A	XP_011539129.1:p.Met318Ile
XM_011540828.1:c.936G>A	XP_011539130.1:p.Met312Ile
XR_246241.1:n.1134G>A
XR_246242.1:n.1118G>A
NM_001319155.1:c.1134G>A	NP_001306084.1:p.Met378Ile
NM_001363587.1:c.936G>A	NP_001350516.1:p.Met312Ile
NR_134988.1:n.935G>A
NR_134989.1:n.1126G>A
NR_134990.1:n.1178-203G>A
NR_134991.1:n.1107G>A
NR_134992.1:n.794-203G>A
NR_134993.1:n.928-203G>A
NR_134994.1:n.1142G>A
XM_017000465.1:c.918G>A	XP_016855954.1:p.Met306Ile
XR_001737005.1:n.1266-203G>A
NM_000778.4:c.1230G>A MANE Select	NP_000769.2:p.Met410Ile
NM_001319155.2:c.1134G>A	NP_001306084.1:p.Met378Ile
NM_001363587.2:c.936G>A	NP_001350516.1:p.Met312Ile
NR_134988.2:n.927G>A
NR_134989.2:n.1118G>A
NR_134990.2:n.1170-203G>A
NR_134991.2:n.1099G>A
NR_134992.2:n.786-203G>A
NR_134993.2:n.920-203G>A
NR_134994.2:n.1134G>A