Canonical Allele Identifier: CA340223235

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398502T>C (hg19) ; chr1:g.46932830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932830T>C , CM000663.2:g.46932830T>C	GRCh38
NC_000001.10:g.47398502T>C , CM000663.1:g.47398502T>C	GRCh37
NC_000001.9:g.47171089T>C	NCBI36
NG_007932.1:g.13655A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1295A>G MANE Select	ENSP00000311095.4:p.Asp432Gly
ENST00000310638.8:c.1295A>G	ENSP00000311095.4:p.Asp432Gly
ENST00000371904.8:c.1298A>G	ENSP00000360971.4:p.Asp433Gly
ENST00000371905.1:c.1295A>G	ENSP00000360972.1:p.Asp432Gly
ENST00000462347.5:c.1001A>G	ENSP00000477495.1:p.Asp334Gly
ENST00000465874.5:c.*93A>G	ENSP00000476368.1:n.*93A>G
ENST00000468629.5:c.1134A>G	ENSP00000476619.1:p.Ter378Trp
ENST00000474458.5:c.750A>G	ENSP00000476988.1:p.Ter250Trp
ENST00000475477.5:c.*89A>G	ENSP00000476854.1:n.*89A>G
NM_000778.3:c.1295A>G	NP_000769.2:p.Asp432Gly
XM_005270539.1:c.1001A>G	XP_005270596.1:p.Asp334Gly
XM_011540826.1:c.1313A>G	XP_011539128.1:p.Asp438Gly
XM_011540827.1:c.1019A>G	XP_011539129.1:p.Asp340Gly
XM_011540828.1:c.1001A>G	XP_011539130.1:p.Asp334Gly
XR_246241.1:n.1199A>G
XR_246242.1:n.1183A>G
NM_001319155.1:c.1199A>G	NP_001306084.1:p.Asp400Gly
NM_001363587.1:c.1001A>G	NP_001350516.1:p.Asp334Gly
NR_134988.1:n.1000A>G
NR_134989.1:n.1191A>G
NR_134990.1:n.1185A>G
NR_134991.1:n.1172A>G
NR_134992.1:n.801A>G
NR_134993.1:n.935A>G
NR_134994.1:n.1207A>G
XM_017000465.1:c.983A>G	XP_016855954.1:p.Asp328Gly
XR_001737005.1:n.1273A>G
NM_000778.4:c.1295A>G MANE Select	NP_000769.2:p.Asp432Gly
NM_001319155.2:c.1199A>G	NP_001306084.1:p.Asp400Gly
NM_001363587.2:c.1001A>G	NP_001350516.1:p.Asp334Gly
NR_134988.2:n.992A>G
NR_134989.2:n.1183A>G
NR_134990.2:n.1177A>G
NR_134991.2:n.1164A>G
NR_134992.2:n.793A>G
NR_134993.2:n.927A>G
NR_134994.2:n.1199A>G