Canonical Allele Identifier: CA340223181

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398473G>T (hg19) ; chr1:g.46932801G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932801G>T , CM000663.2:g.46932801G>T	GRCh38
NC_000001.10:g.47398473G>T , CM000663.1:g.47398473G>T	GRCh37
NC_000001.9:g.47171060G>T	NCBI36
NG_007932.1:g.13684C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1324C>A MANE Select	ENSP00000311095.4:p.Gln442Lys
ENST00000310638.8:c.1324C>A	ENSP00000311095.4:p.Gln442Lys
ENST00000371904.8:c.1327C>A	ENSP00000360971.4:p.Gln443Lys
ENST00000371905.1:c.1324C>A	ENSP00000360972.1:p.Gln442Lys
ENST00000462347.5:c.1030C>A	ENSP00000477495.1:p.Gln344Lys
ENST00000465874.5:c.*122C>A	ENSP00000476368.1:n.*122C>A
ENST00000468629.5:c.*29C>A	ENSP00000476619.1:n.*29C>A
ENST00000474458.5:c.*29C>A	ENSP00000476988.1:n.*29C>A
ENST00000475477.5:c.*118C>A	ENSP00000476854.1:n.*118C>A
NM_000778.3:c.1324C>A	NP_000769.2:p.Gln442Lys
XM_005270539.1:c.1030C>A	XP_005270596.1:p.Gln344Lys
XM_011540826.1:c.1342C>A	XP_011539128.1:p.Gln448Lys
XM_011540827.1:c.1048C>A	XP_011539129.1:p.Gln350Lys
XM_011540828.1:c.1030C>A	XP_011539130.1:p.Gln344Lys
XR_246241.1:n.1228C>A
XR_246242.1:n.1212C>A
NM_001319155.1:c.1228C>A	NP_001306084.1:p.Gln410Lys
NM_001363587.1:c.1030C>A	NP_001350516.1:p.Gln344Lys
NR_134988.1:n.1029C>A
NR_134989.1:n.1220C>A
NR_134990.1:n.1214C>A
NR_134991.1:n.1201C>A
NR_134992.1:n.830C>A
NR_134993.1:n.964C>A
NR_134994.1:n.1236C>A
XM_017000465.1:c.1012C>A	XP_016855954.1:p.Gln338Lys
XR_001737005.1:n.1302C>A
NM_000778.4:c.1324C>A MANE Select	NP_000769.2:p.Gln442Lys
NM_001319155.2:c.1228C>A	NP_001306084.1:p.Gln410Lys
NM_001363587.2:c.1030C>A	NP_001350516.1:p.Gln344Lys
NR_134988.2:n.1021C>A
NR_134989.2:n.1212C>A
NR_134990.2:n.1206C>A
NR_134991.2:n.1193C>A
NR_134992.2:n.822C>A
NR_134993.2:n.956C>A
NR_134994.2:n.1228C>A