Canonical Allele Identifier: CA340223157

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398464G>C (hg19) ; chr1:g.46932792G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932792G>C , CM000663.2:g.46932792G>C	GRCh38
NC_000001.10:g.47398464G>C , CM000663.1:g.47398464G>C	GRCh37
NC_000001.9:g.47171051G>C	NCBI36
NG_007932.1:g.13693C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1333C>G MANE Select	ENSP00000311095.4:p.His445Asp
ENST00000310638.8:c.1333C>G	ENSP00000311095.4:p.His445Asp
ENST00000371904.8:c.1336C>G	ENSP00000360971.4:p.His446Asp
ENST00000371905.1:c.1333C>G	ENSP00000360972.1:p.His445Asp
ENST00000462347.5:c.1039C>G	ENSP00000477495.1:p.His347Asp
ENST00000465874.5:c.*131C>G	ENSP00000476368.1:n.*131C>G
ENST00000468629.5:c.*38C>G	ENSP00000476619.1:n.*38C>G
ENST00000474458.5:c.*38C>G	ENSP00000476988.1:n.*38C>G
ENST00000475477.5:c.*127C>G	ENSP00000476854.1:n.*127C>G
NM_000778.3:c.1333C>G	NP_000769.2:p.His445Asp
XM_005270539.1:c.1039C>G	XP_005270596.1:p.His347Asp
XM_011540826.1:c.1351C>G	XP_011539128.1:p.His451Asp
XM_011540827.1:c.1057C>G	XP_011539129.1:p.His353Asp
XM_011540828.1:c.1039C>G	XP_011539130.1:p.His347Asp
XR_246241.1:n.1237C>G
XR_246242.1:n.1221C>G
NM_001319155.1:c.1237C>G	NP_001306084.1:p.His413Asp
NM_001363587.1:c.1039C>G	NP_001350516.1:p.His347Asp
NR_134988.1:n.1038C>G
NR_134989.1:n.1229C>G
NR_134990.1:n.1223C>G
NR_134991.1:n.1210C>G
NR_134992.1:n.839C>G
NR_134993.1:n.973C>G
NR_134994.1:n.1245C>G
XM_017000465.1:c.1021C>G	XP_016855954.1:p.His341Asp
XR_001737005.1:n.1311C>G
NM_000778.4:c.1333C>G MANE Select	NP_000769.2:p.His445Asp
NM_001319155.2:c.1237C>G	NP_001306084.1:p.His413Asp
NM_001363587.2:c.1039C>G	NP_001350516.1:p.His347Asp
NR_134988.2:n.1030C>G
NR_134989.2:n.1221C>G
NR_134990.2:n.1215C>G
NR_134991.2:n.1202C>G
NR_134992.2:n.831C>G
NR_134993.2:n.965C>G
NR_134994.2:n.1237C>G