Canonical Allele Identifier: CA340223199

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398484G>C (hg19) ; chr1:g.46932812G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932812G>C , CM000663.2:g.46932812G>C	GRCh38
NC_000001.10:g.47398484G>C , CM000663.1:g.47398484G>C	GRCh37
NC_000001.9:g.47171071G>C	NCBI36
NG_007932.1:g.13673C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1313C>G MANE Select	ENSP00000311095.4:p.Pro438Arg
ENST00000310638.8:c.1313C>G	ENSP00000311095.4:p.Pro438Arg
ENST00000371904.8:c.1316C>G	ENSP00000360971.4:p.Pro439Arg
ENST00000371905.1:c.1313C>G	ENSP00000360972.1:p.Pro438Arg
ENST00000462347.5:c.1019C>G	ENSP00000477495.1:p.Pro340Arg
ENST00000465874.5:c.*111C>G	ENSP00000476368.1:n.*111C>G
ENST00000468629.5:c.*18C>G	ENSP00000476619.1:n.*18C>G
ENST00000474458.5:c.*18C>G	ENSP00000476988.1:n.*18C>G
ENST00000475477.5:c.*107C>G	ENSP00000476854.1:n.*107C>G
NM_000778.3:c.1313C>G	NP_000769.2:p.Pro438Arg
XM_005270539.1:c.1019C>G	XP_005270596.1:p.Pro340Arg
XM_011540826.1:c.1331C>G	XP_011539128.1:p.Pro444Arg
XM_011540827.1:c.1037C>G	XP_011539129.1:p.Pro346Arg
XM_011540828.1:c.1019C>G	XP_011539130.1:p.Pro340Arg
XR_246241.1:n.1217C>G
XR_246242.1:n.1201C>G
NM_001319155.1:c.1217C>G	NP_001306084.1:p.Pro406Arg
NM_001363587.1:c.1019C>G	NP_001350516.1:p.Pro340Arg
NR_134988.1:n.1018C>G
NR_134989.1:n.1209C>G
NR_134990.1:n.1203C>G
NR_134991.1:n.1190C>G
NR_134992.1:n.819C>G
NR_134993.1:n.953C>G
NR_134994.1:n.1225C>G
XM_017000465.1:c.1001C>G	XP_016855954.1:p.Pro334Arg
XR_001737005.1:n.1291C>G
NM_000778.4:c.1313C>G MANE Select	NP_000769.2:p.Pro438Arg
NM_001319155.2:c.1217C>G	NP_001306084.1:p.Pro406Arg
NM_001363587.2:c.1019C>G	NP_001350516.1:p.Pro340Arg
NR_134988.2:n.1010C>G
NR_134989.2:n.1201C>G
NR_134990.2:n.1195C>G
NR_134991.2:n.1182C>G
NR_134992.2:n.811C>G
NR_134993.2:n.945C>G
NR_134994.2:n.1217C>G