Canonical Allele Identifier: CA340223222

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398496A>C (hg19) ; chr1:g.46932824A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932824A>C , CM000663.2:g.46932824A>C	GRCh38
NC_000001.10:g.47398496A>C , CM000663.1:g.47398496A>C	GRCh37
NC_000001.9:g.47171083A>C	NCBI36
NG_007932.1:g.13661T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1301T>G MANE Select	ENSP00000311095.4:p.Phe434Cys
ENST00000310638.8:c.1301T>G	ENSP00000311095.4:p.Phe434Cys
ENST00000371904.8:c.1304T>G	ENSP00000360971.4:p.Phe435Cys
ENST00000371905.1:c.1301T>G	ENSP00000360972.1:p.Phe434Cys
ENST00000462347.5:c.1007T>G	ENSP00000477495.1:p.Phe336Cys
ENST00000465874.5:c.*99T>G	ENSP00000476368.1:n.*99T>G
ENST00000468629.5:c.*6T>G	ENSP00000476619.1:n.*6T>G
ENST00000474458.5:c.*6T>G	ENSP00000476988.1:n.*6T>G
ENST00000475477.5:c.*95T>G	ENSP00000476854.1:n.*95T>G
NM_000778.3:c.1301T>G	NP_000769.2:p.Phe434Cys
XM_005270539.1:c.1007T>G	XP_005270596.1:p.Phe336Cys
XM_011540826.1:c.1319T>G	XP_011539128.1:p.Phe440Cys
XM_011540827.1:c.1025T>G	XP_011539129.1:p.Phe342Cys
XM_011540828.1:c.1007T>G	XP_011539130.1:p.Phe336Cys
XR_246241.1:n.1205T>G
XR_246242.1:n.1189T>G
NM_001319155.1:c.1205T>G	NP_001306084.1:p.Phe402Cys
NM_001363587.1:c.1007T>G	NP_001350516.1:p.Phe336Cys
NR_134988.1:n.1006T>G
NR_134989.1:n.1197T>G
NR_134990.1:n.1191T>G
NR_134991.1:n.1178T>G
NR_134992.1:n.807T>G
NR_134993.1:n.941T>G
NR_134994.1:n.1213T>G
XM_017000465.1:c.989T>G	XP_016855954.1:p.Phe330Cys
XR_001737005.1:n.1279T>G
NM_000778.4:c.1301T>G MANE Select	NP_000769.2:p.Phe434Cys
NM_001319155.2:c.1205T>G	NP_001306084.1:p.Phe402Cys
NM_001363587.2:c.1007T>G	NP_001350516.1:p.Phe336Cys
NR_134988.2:n.998T>G
NR_134989.2:n.1189T>G
NR_134990.2:n.1183T>G
NR_134991.2:n.1170T>G
NR_134992.2:n.799T>G
NR_134993.2:n.933T>G
NR_134994.2:n.1205T>G