Canonical Allele Identifier: CA417755733

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398438T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932766T>A , CM000663.2:g.46932766T>A	GRCh38
NC_000001.10:g.47398438T>A , CM000663.1:g.47398438T>A	GRCh37
NC_000001.9:g.47171025T>A	NCBI36
NG_007932.1:g.13719A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1359A>T MANE Select	ENSP00000311095.4:p.Gly453=
ENST00000310638.8:c.1359A>T	ENSP00000311095.4:p.Gly453=
ENST00000371904.8:c.1362A>T	ENSP00000360971.4:p.Gly454=
ENST00000371905.1:c.1359A>T	ENSP00000360972.1:p.Gly453=
ENST00000462347.5:c.1065A>T	ENSP00000477495.1:p.Gly355=
ENST00000465874.5:c.*157A>T	ENSP00000476368.1:n.*157A>T
ENST00000468629.5:c.*64A>T	ENSP00000476619.1:n.*64A>T
ENST00000474458.5:c.*64A>T	ENSP00000476988.1:n.*64A>T
ENST00000475477.5:c.*153A>T	ENSP00000476854.1:n.*153A>T
NM_000778.3:c.1359A>T	NP_000769.2:p.Gly453=
XM_005270539.1:c.1065A>T	XP_005270596.1:p.Gly355=
XM_011540826.1:c.1377A>T	XP_011539128.1:p.Gly459=
XM_011540827.1:c.1083A>T	XP_011539129.1:p.Gly361=
XM_011540828.1:c.1065A>T	XP_011539130.1:p.Gly355=
XR_246241.1:n.1263A>T
XR_246242.1:n.1247A>T
NM_001319155.1:c.1263A>T	NP_001306084.1:p.Gly421=
NM_001363587.1:c.1065A>T	NP_001350516.1:p.Gly355=
NR_134988.1:n.1064A>T
NR_134989.1:n.1255A>T
NR_134990.1:n.1249A>T
NR_134991.1:n.1236A>T
NR_134992.1:n.865A>T
NR_134993.1:n.999A>T
NR_134994.1:n.1271A>T
XM_017000465.1:c.1047A>T	XP_016855954.1:p.Gly349=
XR_001737005.1:n.1337A>T
NM_000778.4:c.1359A>T MANE Select	NP_000769.2:p.Gly453=
NM_001319155.2:c.1263A>T	NP_001306084.1:p.Gly421=
NM_001363587.2:c.1065A>T	NP_001350516.1:p.Gly355=
NR_134988.2:n.1056A>T
NR_134989.2:n.1247A>T
NR_134990.2:n.1241A>T
NR_134991.2:n.1228A>T
NR_134992.2:n.857A>T
NR_134993.2:n.991A>T
NR_134994.2:n.1263A>T