Canonical Allele Identifier: CA340223173

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398470G>A (hg19) ; chr1:g.46932798G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932798G>A , CM000663.2:g.46932798G>A	GRCh38
NC_000001.10:g.47398470G>A , CM000663.1:g.47398470G>A	GRCh37
NC_000001.9:g.47171057G>A	NCBI36
NG_007932.1:g.13687C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1327C>T MANE Select	ENSP00000311095.4:p.His443Tyr
ENST00000310638.8:c.1327C>T	ENSP00000311095.4:p.His443Tyr
ENST00000371904.8:c.1330C>T	ENSP00000360971.4:p.His444Tyr
ENST00000371905.1:c.1327C>T	ENSP00000360972.1:p.His443Tyr
ENST00000462347.5:c.1033C>T	ENSP00000477495.1:p.His345Tyr
ENST00000465874.5:c.*125C>T	ENSP00000476368.1:n.*125C>T
ENST00000468629.5:c.*32C>T	ENSP00000476619.1:n.*32C>T
ENST00000474458.5:c.*32C>T	ENSP00000476988.1:n.*32C>T
ENST00000475477.5:c.*121C>T	ENSP00000476854.1:n.*121C>T
NM_000778.3:c.1327C>T	NP_000769.2:p.His443Tyr
XM_005270539.1:c.1033C>T	XP_005270596.1:p.His345Tyr
XM_011540826.1:c.1345C>T	XP_011539128.1:p.His449Tyr
XM_011540827.1:c.1051C>T	XP_011539129.1:p.His351Tyr
XM_011540828.1:c.1033C>T	XP_011539130.1:p.His345Tyr
XR_246241.1:n.1231C>T
XR_246242.1:n.1215C>T
NM_001319155.1:c.1231C>T	NP_001306084.1:p.His411Tyr
NM_001363587.1:c.1033C>T	NP_001350516.1:p.His345Tyr
NR_134988.1:n.1032C>T
NR_134989.1:n.1223C>T
NR_134990.1:n.1217C>T
NR_134991.1:n.1204C>T
NR_134992.1:n.833C>T
NR_134993.1:n.967C>T
NR_134994.1:n.1239C>T
XM_017000465.1:c.1015C>T	XP_016855954.1:p.His339Tyr
XR_001737005.1:n.1305C>T
NM_000778.4:c.1327C>T MANE Select	NP_000769.2:p.His443Tyr
NM_001319155.2:c.1231C>T	NP_001306084.1:p.His411Tyr
NM_001363587.2:c.1033C>T	NP_001350516.1:p.His345Tyr
NR_134988.2:n.1024C>T
NR_134989.2:n.1215C>T
NR_134990.2:n.1209C>T
NR_134991.2:n.1196C>T
NR_134992.2:n.825C>T
NR_134993.2:n.959C>T
NR_134994.2:n.1231C>T