Canonical Allele Identifier: CA340223320

Gene: CYP4A11

Linked Data

• dbSNP Id: rs2148454180
• MyVariant Identifiers: chr1:g.47398682G>C (hg19) ; chr1:g.46933010G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933010G>C , CM000663.2:g.46933010G>C	GRCh38
NC_000001.10:g.47398682G>C , CM000663.1:g.47398682G>C	GRCh37
NC_000001.9:g.47171269G>C	NCBI36
NG_007932.1:g.13475C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1260C>G MANE Select	ENSP00000311095.4:p.His420Gln
ENST00000310638.8:c.1260C>G	ENSP00000311095.4:p.His420Gln
ENST00000371904.8:c.1263C>G	ENSP00000360971.4:p.His421Gln
ENST00000371905.1:c.1260C>G	ENSP00000360972.1:p.His420Gln
ENST00000462347.5:c.966C>G	ENSP00000477495.1:p.His322Gln
ENST00000465874.5:c.*58C>G	ENSP00000476368.1:n.*58C>G
ENST00000468629.5:c.1127-173C>G	ENSP00000476619.1:n.1127-173C>G
ENST00000474458.5:c.743-173C>G	ENSP00000476988.1:n.743-173C>G
ENST00000475477.5:c.*82-173C>G	ENSP00000476854.1:n.*82-173C>G
NM_000778.3:c.1260C>G	NP_000769.2:p.His420Gln
XM_005270539.1:c.966C>G	XP_005270596.1:p.His322Gln
XM_011540826.1:c.1278C>G	XP_011539128.1:p.His426Gln
XM_011540827.1:c.984C>G	XP_011539129.1:p.His328Gln
XM_011540828.1:c.966C>G	XP_011539130.1:p.His322Gln
XR_246241.1:n.1164C>G
XR_246242.1:n.1148C>G
NM_001319155.1:c.1164C>G	NP_001306084.1:p.His388Gln
NM_001363587.1:c.966C>G	NP_001350516.1:p.His322Gln
NR_134988.1:n.965C>G
NR_134989.1:n.1156C>G
NR_134990.1:n.1178-173C>G
NR_134991.1:n.1137C>G
NR_134992.1:n.794-173C>G
NR_134993.1:n.928-173C>G
NR_134994.1:n.1172C>G
XM_017000465.1:c.948C>G	XP_016855954.1:p.His316Gln
XR_001737005.1:n.1266-173C>G
NM_000778.4:c.1260C>G MANE Select	NP_000769.2:p.His420Gln
NM_001319155.2:c.1164C>G	NP_001306084.1:p.His388Gln
NM_001363587.2:c.966C>G	NP_001350516.1:p.His322Gln
NR_134988.2:n.957C>G
NR_134989.2:n.1148C>G
NR_134990.2:n.1170-173C>G
NR_134991.2:n.1129C>G
NR_134992.2:n.786-173C>G
NR_134993.2:n.920-173C>G
NR_134994.2:n.1164C>G