Canonical Allele Identifier: CA340223313

Gene: CYP4A11

Linked Data

• dbSNP Id: rs2148454170
• MyVariant Identifiers: chr1:g.47398680T>A (hg19) ; chr1:g.46933008T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933008T>A , CM000663.2:g.46933008T>A	GRCh38
NC_000001.10:g.47398680T>A , CM000663.1:g.47398680T>A	GRCh37
NC_000001.9:g.47171267T>A	NCBI36
NG_007932.1:g.13477A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1262A>T MANE Select	ENSP00000311095.4:p.Asn421Ile
ENST00000310638.8:c.1262A>T	ENSP00000311095.4:p.Asn421Ile
ENST00000371904.8:c.1265A>T	ENSP00000360971.4:p.Asn422Ile
ENST00000371905.1:c.1262A>T	ENSP00000360972.1:p.Asn421Ile
ENST00000462347.5:c.968A>T	ENSP00000477495.1:p.Asn323Ile
ENST00000465874.5:c.*60A>T	ENSP00000476368.1:n.*60A>T
ENST00000468629.5:c.1127-171A>T	ENSP00000476619.1:n.1127-171A>T
ENST00000474458.5:c.743-171A>T	ENSP00000476988.1:n.743-171A>T
ENST00000475477.5:c.*82-171A>T	ENSP00000476854.1:n.*82-171A>T
NM_000778.3:c.1262A>T	NP_000769.2:p.Asn421Ile
XM_005270539.1:c.968A>T	XP_005270596.1:p.Asn323Ile
XM_011540826.1:c.1280A>T	XP_011539128.1:p.Asn427Ile
XM_011540827.1:c.986A>T	XP_011539129.1:p.Asn329Ile
XM_011540828.1:c.968A>T	XP_011539130.1:p.Asn323Ile
XR_246241.1:n.1166A>T
XR_246242.1:n.1150A>T
NM_001319155.1:c.1166A>T	NP_001306084.1:p.Asn389Ile
NM_001363587.1:c.968A>T	NP_001350516.1:p.Asn323Ile
NR_134988.1:n.967A>T
NR_134989.1:n.1158A>T
NR_134990.1:n.1178-171A>T
NR_134991.1:n.1139A>T
NR_134992.1:n.794-171A>T
NR_134993.1:n.928-171A>T
NR_134994.1:n.1174A>T
XM_017000465.1:c.950A>T	XP_016855954.1:p.Asn317Ile
XR_001737005.1:n.1266-171A>T
NM_000778.4:c.1262A>T MANE Select	NP_000769.2:p.Asn421Ile
NM_001319155.2:c.1166A>T	NP_001306084.1:p.Asn389Ile
NM_001363587.2:c.968A>T	NP_001350516.1:p.Asn323Ile
NR_134988.2:n.959A>T
NR_134989.2:n.1150A>T
NR_134990.2:n.1170-171A>T
NR_134991.2:n.1131A>T
NR_134992.2:n.786-171A>T
NR_134993.2:n.920-171A>T
NR_134994.2:n.1166A>T