Canonical Allele Identifier: CA340223122

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398448A>C (hg19) ; chr1:g.46932776A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932776A>C , CM000663.2:g.46932776A>C	GRCh38
NC_000001.10:g.47398448A>C , CM000663.1:g.47398448A>C	GRCh37
NC_000001.9:g.47171035A>C	NCBI36
NG_007932.1:g.13709T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1349T>G MANE Select	ENSP00000311095.4:p.Phe450Cys
ENST00000310638.8:c.1349T>G	ENSP00000311095.4:p.Phe450Cys
ENST00000371904.8:c.1352T>G	ENSP00000360971.4:p.Phe451Cys
ENST00000371905.1:c.1349T>G	ENSP00000360972.1:p.Phe450Cys
ENST00000462347.5:c.1055T>G	ENSP00000477495.1:p.Phe352Cys
ENST00000465874.5:c.*147T>G	ENSP00000476368.1:n.*147T>G
ENST00000468629.5:c.*54T>G	ENSP00000476619.1:n.*54T>G
ENST00000474458.5:c.*54T>G	ENSP00000476988.1:n.*54T>G
ENST00000475477.5:c.*143T>G	ENSP00000476854.1:n.*143T>G
NM_000778.3:c.1349T>G	NP_000769.2:p.Phe450Cys
XM_005270539.1:c.1055T>G	XP_005270596.1:p.Phe352Cys
XM_011540826.1:c.1367T>G	XP_011539128.1:p.Phe456Cys
XM_011540827.1:c.1073T>G	XP_011539129.1:p.Phe358Cys
XM_011540828.1:c.1055T>G	XP_011539130.1:p.Phe352Cys
XR_246241.1:n.1253T>G
XR_246242.1:n.1237T>G
NM_001319155.1:c.1253T>G	NP_001306084.1:p.Phe418Cys
NM_001363587.1:c.1055T>G	NP_001350516.1:p.Phe352Cys
NR_134988.1:n.1054T>G
NR_134989.1:n.1245T>G
NR_134990.1:n.1239T>G
NR_134991.1:n.1226T>G
NR_134992.1:n.855T>G
NR_134993.1:n.989T>G
NR_134994.1:n.1261T>G
XM_017000465.1:c.1037T>G	XP_016855954.1:p.Phe346Cys
XR_001737005.1:n.1327T>G
NM_000778.4:c.1349T>G MANE Select	NP_000769.2:p.Phe450Cys
NM_001319155.2:c.1253T>G	NP_001306084.1:p.Phe418Cys
NM_001363587.2:c.1055T>G	NP_001350516.1:p.Phe352Cys
NR_134988.2:n.1046T>G
NR_134989.2:n.1237T>G
NR_134990.2:n.1231T>G
NR_134991.2:n.1218T>G
NR_134992.2:n.847T>G
NR_134993.2:n.981T>G
NR_134994.2:n.1253T>G