Canonical Allele Identifier: CA417755835

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398477A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932805A>G , CM000663.2:g.46932805A>G	GRCh38
NC_000001.10:g.47398477A>G , CM000663.1:g.47398477A>G	GRCh37
NC_000001.9:g.47171064A>G	NCBI36
NG_007932.1:g.13680T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1320T>C MANE Select	ENSP00000311095.4:p.Ser440=
ENST00000310638.8:c.1320T>C	ENSP00000311095.4:p.Ser440=
ENST00000371904.8:c.1323T>C	ENSP00000360971.4:p.Ser441=
ENST00000371905.1:c.1320T>C	ENSP00000360972.1:p.Ser440=
ENST00000462347.5:c.1026T>C	ENSP00000477495.1:p.Ser342=
ENST00000465874.5:c.*118T>C	ENSP00000476368.1:n.*118T>C
ENST00000468629.5:c.*25T>C	ENSP00000476619.1:n.*25T>C
ENST00000474458.5:c.*25T>C	ENSP00000476988.1:n.*25T>C
ENST00000475477.5:c.*114T>C	ENSP00000476854.1:n.*114T>C
NM_000778.3:c.1320T>C	NP_000769.2:p.Ser440=
XM_005270539.1:c.1026T>C	XP_005270596.1:p.Ser342=
XM_011540826.1:c.1338T>C	XP_011539128.1:p.Ser446=
XM_011540827.1:c.1044T>C	XP_011539129.1:p.Ser348=
XM_011540828.1:c.1026T>C	XP_011539130.1:p.Ser342=
XR_246241.1:n.1224T>C
XR_246242.1:n.1208T>C
NM_001319155.1:c.1224T>C	NP_001306084.1:p.Ser408=
NM_001363587.1:c.1026T>C	NP_001350516.1:p.Ser342=
NR_134988.1:n.1025T>C
NR_134989.1:n.1216T>C
NR_134990.1:n.1210T>C
NR_134991.1:n.1197T>C
NR_134992.1:n.826T>C
NR_134993.1:n.960T>C
NR_134994.1:n.1232T>C
XM_017000465.1:c.1008T>C	XP_016855954.1:p.Ser336=
XR_001737005.1:n.1298T>C
NM_000778.4:c.1320T>C MANE Select	NP_000769.2:p.Ser440=
NM_001319155.2:c.1224T>C	NP_001306084.1:p.Ser408=
NM_001363587.2:c.1026T>C	NP_001350516.1:p.Ser342=
NR_134988.2:n.1017T>C
NR_134989.2:n.1208T>C
NR_134990.2:n.1202T>C
NR_134991.2:n.1189T>C
NR_134992.2:n.818T>C
NR_134993.2:n.952T>C
NR_134994.2:n.1224T>C