Canonical Allele Identifier: CA340223340

Gene: CYP4A11

Linked Data

• dbSNP Id: rs2148454234
• MyVariant Identifiers: chr1:g.47398692C>A (hg19) ; chr1:g.46933020C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933020C>A , CM000663.2:g.46933020C>A	GRCh38
NC_000001.10:g.47398692C>A , CM000663.1:g.47398692C>A	GRCh37
NC_000001.9:g.47171279C>A	NCBI36
NG_007932.1:g.13465G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1250G>T MANE Select	ENSP00000311095.4:p.Gly417Val
ENST00000310638.8:c.1250G>T	ENSP00000311095.4:p.Gly417Val
ENST00000371904.8:c.1253G>T	ENSP00000360971.4:p.Gly418Val
ENST00000371905.1:c.1250G>T	ENSP00000360972.1:p.Gly417Val
ENST00000462347.5:c.956G>T	ENSP00000477495.1:p.Gly319Val
ENST00000465874.5:c.*48G>T	ENSP00000476368.1:n.*48G>T
ENST00000468629.5:c.1127-183G>T	ENSP00000476619.1:n.1127-183G>T
ENST00000474458.5:c.743-183G>T	ENSP00000476988.1:n.743-183G>T
ENST00000475477.5:c.*82-183G>T	ENSP00000476854.1:n.*82-183G>T
NM_000778.3:c.1250G>T	NP_000769.2:p.Gly417Val
XM_005270539.1:c.956G>T	XP_005270596.1:p.Gly319Val
XM_011540826.1:c.1268G>T	XP_011539128.1:p.Gly423Val
XM_011540827.1:c.974G>T	XP_011539129.1:p.Gly325Val
XM_011540828.1:c.956G>T	XP_011539130.1:p.Gly319Val
XR_246241.1:n.1154G>T
XR_246242.1:n.1138G>T
NM_001319155.1:c.1154G>T	NP_001306084.1:p.Gly385Val
NM_001363587.1:c.956G>T	NP_001350516.1:p.Gly319Val
NR_134988.1:n.955G>T
NR_134989.1:n.1146G>T
NR_134990.1:n.1178-183G>T
NR_134991.1:n.1127G>T
NR_134992.1:n.794-183G>T
NR_134993.1:n.928-183G>T
NR_134994.1:n.1162G>T
XM_017000465.1:c.938G>T	XP_016855954.1:p.Gly313Val
XR_001737005.1:n.1266-183G>T
NM_000778.4:c.1250G>T MANE Select	NP_000769.2:p.Gly417Val
NM_001319155.2:c.1154G>T	NP_001306084.1:p.Gly385Val
NM_001363587.2:c.956G>T	NP_001350516.1:p.Gly319Val
NR_134988.2:n.947G>T
NR_134989.2:n.1138G>T
NR_134990.2:n.1170-183G>T
NR_134991.2:n.1119G>T
NR_134992.2:n.786-183G>T
NR_134993.2:n.920-183G>T
NR_134994.2:n.1154G>T