Canonical Allele Identifier: CA417755736

Gene: CYP4A11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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