Canonical Allele Identifier: CA340223236

Gene: CYP4A11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1295A>C MANE Select	ENSP00000311095.4:p.Asp432Ala
ENST00000310638.8:c.1295A>C	ENSP00000311095.4:p.Asp432Ala
ENST00000371904.8:c.1298A>C	ENSP00000360971.4:p.Asp433Ala
ENST00000371905.1:c.1295A>C	ENSP00000360972.1:p.Asp432Ala
ENST00000462347.5:c.1001A>C	ENSP00000477495.1:p.Asp334Ala
ENST00000465874.5:c.*93A>C	ENSP00000476368.1:n.*93A>C
ENST00000468629.5:c.1134A>C	ENSP00000476619.1:p.Ter378Cys
ENST00000474458.5:c.750A>C	ENSP00000476988.1:p.Ter250Cys
ENST00000475477.5:c.*89A>C	ENSP00000476854.1:n.*89A>C
NM_000778.3:c.1295A>C	NP_000769.2:p.Asp432Ala
XM_005270539.1:c.1001A>C	XP_005270596.1:p.Asp334Ala
XM_011540826.1:c.1313A>C	XP_011539128.1:p.Asp438Ala
XM_011540827.1:c.1019A>C	XP_011539129.1:p.Asp340Ala
XM_011540828.1:c.1001A>C	XP_011539130.1:p.Asp334Ala
XR_246241.1:n.1199A>C
XR_246242.1:n.1183A>C
NM_001319155.1:c.1199A>C	NP_001306084.1:p.Asp400Ala
NM_001363587.1:c.1001A>C	NP_001350516.1:p.Asp334Ala
NR_134988.1:n.1000A>C
NR_134989.1:n.1191A>C
NR_134990.1:n.1185A>C
NR_134991.1:n.1172A>C
NR_134992.1:n.801A>C
NR_134993.1:n.935A>C
NR_134994.1:n.1207A>C
XM_017000465.1:c.983A>C	XP_016855954.1:p.Asp328Ala
XR_001737005.1:n.1273A>C
NM_000778.4:c.1295A>C MANE Select	NP_000769.2:p.Asp432Ala
NM_001319155.2:c.1199A>C	NP_001306084.1:p.Asp400Ala
NM_001363587.2:c.1001A>C	NP_001350516.1:p.Asp334Ala
NR_134988.2:n.992A>C
NR_134989.2:n.1183A>C
NR_134990.2:n.1177A>C
NR_134991.2:n.1164A>C
NR_134992.2:n.793A>C
NR_134993.2:n.927A>C
NR_134994.2:n.1199A>C