Canonical Allele Identifier: CA417755827

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398474A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932802A>C , CM000663.2:g.46932802A>C	GRCh38
NC_000001.10:g.47398474A>C , CM000663.1:g.47398474A>C	GRCh37
NC_000001.9:g.47171061A>C	NCBI36
NG_007932.1:g.13683T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1323T>G MANE Select	ENSP00000311095.4:p.Ala441=
ENST00000310638.8:c.1323T>G	ENSP00000311095.4:p.Ala441=
ENST00000371904.8:c.1326T>G	ENSP00000360971.4:p.Ala442=
ENST00000371905.1:c.1323T>G	ENSP00000360972.1:p.Ala441=
ENST00000462347.5:c.1029T>G	ENSP00000477495.1:p.Ala343=
ENST00000465874.5:c.*121T>G	ENSP00000476368.1:n.*121T>G
ENST00000468629.5:c.*28T>G	ENSP00000476619.1:n.*28T>G
ENST00000474458.5:c.*28T>G	ENSP00000476988.1:n.*28T>G
ENST00000475477.5:c.*117T>G	ENSP00000476854.1:n.*117T>G
NM_000778.3:c.1323T>G	NP_000769.2:p.Ala441=
XM_005270539.1:c.1029T>G	XP_005270596.1:p.Ala343=
XM_011540826.1:c.1341T>G	XP_011539128.1:p.Ala447=
XM_011540827.1:c.1047T>G	XP_011539129.1:p.Ala349=
XM_011540828.1:c.1029T>G	XP_011539130.1:p.Ala343=
XR_246241.1:n.1227T>G
XR_246242.1:n.1211T>G
NM_001319155.1:c.1227T>G	NP_001306084.1:p.Ala409=
NM_001363587.1:c.1029T>G	NP_001350516.1:p.Ala343=
NR_134988.1:n.1028T>G
NR_134989.1:n.1219T>G
NR_134990.1:n.1213T>G
NR_134991.1:n.1200T>G
NR_134992.1:n.829T>G
NR_134993.1:n.963T>G
NR_134994.1:n.1235T>G
XM_017000465.1:c.1011T>G	XP_016855954.1:p.Ala337=
XR_001737005.1:n.1301T>G
NM_000778.4:c.1323T>G MANE Select	NP_000769.2:p.Ala441=
NM_001319155.2:c.1227T>G	NP_001306084.1:p.Ala409=
NM_001363587.2:c.1029T>G	NP_001350516.1:p.Ala343=
NR_134988.2:n.1020T>G
NR_134989.2:n.1211T>G
NR_134990.2:n.1205T>G
NR_134991.2:n.1192T>G
NR_134992.2:n.821T>G
NR_134993.2:n.955T>G
NR_134994.2:n.1227T>G