Canonical Allele Identifier: CA340223247

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398508A>C (hg19) ; chr1:g.46932836A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932836A>C , CM000663.2:g.46932836A>C	GRCh38
NC_000001.10:g.47398508A>C , CM000663.1:g.47398508A>C	GRCh37
NC_000001.9:g.47171095A>C	NCBI36
NG_007932.1:g.13649T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1289T>G MANE Select	ENSP00000311095.4:p.Val430Gly
ENST00000310638.8:c.1289T>G	ENSP00000311095.4:p.Val430Gly
ENST00000371904.8:c.1292T>G	ENSP00000360971.4:p.Val431Gly
ENST00000371905.1:c.1289T>G	ENSP00000360972.1:p.Val430Gly
ENST00000462347.5:c.995T>G	ENSP00000477495.1:p.Val332Gly
ENST00000465874.5:c.*87T>G	ENSP00000476368.1:n.*87T>G
ENST00000468629.5:c.1128T>G	ENSP00000476619.1:p.Gly376=
ENST00000474458.5:c.744T>G	ENSP00000476988.1:p.Ser248Arg
ENST00000475477.5:c.*83T>G	ENSP00000476854.1:n.*83T>G
NM_000778.3:c.1289T>G	NP_000769.2:p.Val430Gly
XM_005270539.1:c.995T>G	XP_005270596.1:p.Val332Gly
XM_011540826.1:c.1307T>G	XP_011539128.1:p.Val436Gly
XM_011540827.1:c.1013T>G	XP_011539129.1:p.Val338Gly
XM_011540828.1:c.995T>G	XP_011539130.1:p.Val332Gly
XR_246241.1:n.1193T>G
XR_246242.1:n.1177T>G
NM_001319155.1:c.1193T>G	NP_001306084.1:p.Val398Gly
NM_001363587.1:c.995T>G	NP_001350516.1:p.Val332Gly
NR_134988.1:n.994T>G
NR_134989.1:n.1185T>G
NR_134990.1:n.1179T>G
NR_134991.1:n.1166T>G
NR_134992.1:n.795T>G
NR_134993.1:n.929T>G
NR_134994.1:n.1201T>G
XM_017000465.1:c.977T>G	XP_016855954.1:p.Val326Gly
XR_001737005.1:n.1267T>G
NM_000778.4:c.1289T>G MANE Select	NP_000769.2:p.Val430Gly
NM_001319155.2:c.1193T>G	NP_001306084.1:p.Val398Gly
NM_001363587.2:c.995T>G	NP_001350516.1:p.Val332Gly
NR_134988.2:n.986T>G
NR_134989.2:n.1177T>G
NR_134990.2:n.1171T>G
NR_134991.2:n.1158T>G
NR_134992.2:n.787T>G
NR_134993.2:n.921T>G
NR_134994.2:n.1193T>G