Canonical Allele Identifier: CA417755932

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398658T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932986T>G , CM000663.2:g.46932986T>G	GRCh38
NC_000001.10:g.47398658T>G , CM000663.1:g.47398658T>G	GRCh37
NC_000001.9:g.47171245T>G	NCBI36
NG_007932.1:g.13499A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1284A>C MANE Select	ENSP00000311095.4:p.Pro428=
ENST00000310638.8:c.1284A>C	ENSP00000311095.4:p.Pro428=
ENST00000371904.8:c.1287A>C	ENSP00000360971.4:p.Pro429=
ENST00000371905.1:c.1284A>C	ENSP00000360972.1:p.Pro428=
ENST00000462347.5:c.990A>C	ENSP00000477495.1:p.Pro330=
ENST00000465874.5:c.*82A>C	ENSP00000476368.1:n.*82A>C
ENST00000468629.5:c.1127-149A>C	ENSP00000476619.1:n.1127-149A>C
ENST00000474458.5:c.743-149A>C	ENSP00000476988.1:n.743-149A>C
ENST00000475477.5:c.*82-149A>C	ENSP00000476854.1:n.*82-149A>C
NM_000778.3:c.1284A>C	NP_000769.2:p.Pro428=
XM_005270539.1:c.990A>C	XP_005270596.1:p.Pro330=
XM_011540826.1:c.1302A>C	XP_011539128.1:p.Pro434=
XM_011540827.1:c.1008A>C	XP_011539129.1:p.Pro336=
XM_011540828.1:c.990A>C	XP_011539130.1:p.Pro330=
XR_246241.1:n.1188A>C
XR_246242.1:n.1172A>C
NM_001319155.1:c.1188A>C	NP_001306084.1:p.Pro396=
NM_001363587.1:c.990A>C	NP_001350516.1:p.Pro330=
NR_134988.1:n.989A>C
NR_134989.1:n.1180A>C
NR_134990.1:n.1178-149A>C
NR_134991.1:n.1161A>C
NR_134992.1:n.794-149A>C
NR_134993.1:n.928-149A>C
NR_134994.1:n.1196A>C
XM_017000465.1:c.972A>C	XP_016855954.1:p.Pro324=
XR_001737005.1:n.1266-149A>C
NM_000778.4:c.1284A>C MANE Select	NP_000769.2:p.Pro428=
NM_001319155.2:c.1188A>C	NP_001306084.1:p.Pro396=
NM_001363587.2:c.990A>C	NP_001350516.1:p.Pro330=
NR_134988.2:n.981A>C
NR_134989.2:n.1172A>C
NR_134990.2:n.1170-149A>C
NR_134991.2:n.1153A>C
NR_134992.2:n.786-149A>C
NR_134993.2:n.920-149A>C
NR_134994.2:n.1188A>C