Canonical Allele Identifier: CA340223130

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1681103112
• MyVariant Identifiers: chr1:g.47398451G>A (hg19) ; chr1:g.46932779G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932779G>A , CM000663.2:g.46932779G>A	GRCh38
NC_000001.10:g.47398451G>A , CM000663.1:g.47398451G>A	GRCh37
NC_000001.9:g.47171038G>A	NCBI36
NG_007932.1:g.13706C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1346C>T MANE Select	ENSP00000311095.4:p.Pro449Leu
ENST00000310638.8:c.1346C>T	ENSP00000311095.4:p.Pro449Leu
ENST00000371904.8:c.1349C>T	ENSP00000360971.4:p.Pro450Leu
ENST00000371905.1:c.1346C>T	ENSP00000360972.1:p.Pro449Leu
ENST00000462347.5:c.1052C>T	ENSP00000477495.1:p.Pro351Leu
ENST00000465874.5:c.*144C>T	ENSP00000476368.1:n.*144C>T
ENST00000468629.5:c.*51C>T	ENSP00000476619.1:n.*51C>T
ENST00000474458.5:c.*51C>T	ENSP00000476988.1:n.*51C>T
ENST00000475477.5:c.*140C>T	ENSP00000476854.1:n.*140C>T
NM_000778.3:c.1346C>T	NP_000769.2:p.Pro449Leu
XM_005270539.1:c.1052C>T	XP_005270596.1:p.Pro351Leu
XM_011540826.1:c.1364C>T	XP_011539128.1:p.Pro455Leu
XM_011540827.1:c.1070C>T	XP_011539129.1:p.Pro357Leu
XM_011540828.1:c.1052C>T	XP_011539130.1:p.Pro351Leu
XR_246241.1:n.1250C>T
XR_246242.1:n.1234C>T
NM_001319155.1:c.1250C>T	NP_001306084.1:p.Pro417Leu
NM_001363587.1:c.1052C>T	NP_001350516.1:p.Pro351Leu
NR_134988.1:n.1051C>T
NR_134989.1:n.1242C>T
NR_134990.1:n.1236C>T
NR_134991.1:n.1223C>T
NR_134992.1:n.852C>T
NR_134993.1:n.986C>T
NR_134994.1:n.1258C>T
XM_017000465.1:c.1034C>T	XP_016855954.1:p.Pro345Leu
XR_001737005.1:n.1324C>T
NM_000778.4:c.1346C>T MANE Select	NP_000769.2:p.Pro449Leu
NM_001319155.2:c.1250C>T	NP_001306084.1:p.Pro417Leu
NM_001363587.2:c.1052C>T	NP_001350516.1:p.Pro351Leu
NR_134988.2:n.1043C>T
NR_134989.2:n.1234C>T
NR_134990.2:n.1228C>T
NR_134991.2:n.1215C>T
NR_134992.2:n.844C>T
NR_134993.2:n.978C>T
NR_134994.2:n.1250C>T