Canonical Allele Identifier: CA340223129

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398451G>T (hg19) ; chr1:g.46932779G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1346C>A MANE Select	ENSP00000311095.4:p.Pro449His
ENST00000310638.8:c.1346C>A	ENSP00000311095.4:p.Pro449His
ENST00000371904.8:c.1349C>A	ENSP00000360971.4:p.Pro450His
ENST00000371905.1:c.1346C>A	ENSP00000360972.1:p.Pro449His
ENST00000462347.5:c.1052C>A	ENSP00000477495.1:p.Pro351His
ENST00000465874.5:c.*144C>A	ENSP00000476368.1:n.*144C>A
ENST00000468629.5:c.*51C>A	ENSP00000476619.1:n.*51C>A
ENST00000474458.5:c.*51C>A	ENSP00000476988.1:n.*51C>A
ENST00000475477.5:c.*140C>A	ENSP00000476854.1:n.*140C>A
NM_000778.3:c.1346C>A	NP_000769.2:p.Pro449His
XM_005270539.1:c.1052C>A	XP_005270596.1:p.Pro351His
XM_011540826.1:c.1364C>A	XP_011539128.1:p.Pro455His
XM_011540827.1:c.1070C>A	XP_011539129.1:p.Pro357His
XM_011540828.1:c.1052C>A	XP_011539130.1:p.Pro351His
XR_246241.1:n.1250C>A
XR_246242.1:n.1234C>A
NM_001319155.1:c.1250C>A	NP_001306084.1:p.Pro417His
NM_001363587.1:c.1052C>A	NP_001350516.1:p.Pro351His
NR_134988.1:n.1051C>A
NR_134989.1:n.1242C>A
NR_134990.1:n.1236C>A
NR_134991.1:n.1223C>A
NR_134992.1:n.852C>A
NR_134993.1:n.986C>A
NR_134994.1:n.1258C>A
XM_017000465.1:c.1034C>A	XP_016855954.1:p.Pro345His
XR_001737005.1:n.1324C>A
NM_000778.4:c.1346C>A MANE Select	NP_000769.2:p.Pro449His
NM_001319155.2:c.1250C>A	NP_001306084.1:p.Pro417His
NM_001363587.2:c.1052C>A	NP_001350516.1:p.Pro351His
NR_134988.2:n.1043C>A
NR_134989.2:n.1234C>A
NR_134990.2:n.1228C>A
NR_134991.2:n.1215C>A
NR_134992.2:n.844C>A
NR_134993.2:n.978C>A
NR_134994.2:n.1250C>A