Canonical Allele Identifier: CA340223376

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398710A>G (hg19) ; chr1:g.46933038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933038A>G , CM000663.2:g.46933038A>G	GRCh38
NC_000001.10:g.47398710A>G , CM000663.1:g.47398710A>G	GRCh37
NC_000001.9:g.47171297A>G	NCBI36
NG_007932.1:g.13447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1232T>C MANE Select	ENSP00000311095.4:p.Val411Ala
ENST00000310638.8:c.1232T>C	ENSP00000311095.4:p.Val411Ala
ENST00000371904.8:c.1235T>C	ENSP00000360971.4:p.Val412Ala
ENST00000371905.1:c.1232T>C	ENSP00000360972.1:p.Val411Ala
ENST00000462347.5:c.938T>C	ENSP00000477495.1:p.Val313Ala
ENST00000465874.5:c.*30T>C	ENSP00000476368.1:n.*30T>C
ENST00000468629.5:c.1127-201T>C	ENSP00000476619.1:n.1127-201T>C
ENST00000474458.5:c.743-201T>C	ENSP00000476988.1:n.743-201T>C
ENST00000475477.5:c.*82-201T>C	ENSP00000476854.1:n.*82-201T>C
NM_000778.3:c.1232T>C	NP_000769.2:p.Val411Ala
XM_005270539.1:c.938T>C	XP_005270596.1:p.Val313Ala
XM_011540826.1:c.1250T>C	XP_011539128.1:p.Val417Ala
XM_011540827.1:c.956T>C	XP_011539129.1:p.Val319Ala
XM_011540828.1:c.938T>C	XP_011539130.1:p.Val313Ala
XR_246241.1:n.1136T>C
XR_246242.1:n.1120T>C
NM_001319155.1:c.1136T>C	NP_001306084.1:p.Val379Ala
NM_001363587.1:c.938T>C	NP_001350516.1:p.Val313Ala
NR_134988.1:n.937T>C
NR_134989.1:n.1128T>C
NR_134990.1:n.1178-201T>C
NR_134991.1:n.1109T>C
NR_134992.1:n.794-201T>C
NR_134993.1:n.928-201T>C
NR_134994.1:n.1144T>C
XM_017000465.1:c.920T>C	XP_016855954.1:p.Val307Ala
XR_001737005.1:n.1266-201T>C
NM_000778.4:c.1232T>C MANE Select	NP_000769.2:p.Val411Ala
NM_001319155.2:c.1136T>C	NP_001306084.1:p.Val379Ala
NM_001363587.2:c.938T>C	NP_001350516.1:p.Val313Ala
NR_134988.2:n.929T>C
NR_134989.2:n.1120T>C
NR_134990.2:n.1170-201T>C
NR_134991.2:n.1101T>C
NR_134992.2:n.786-201T>C
NR_134993.2:n.920-201T>C
NR_134994.2:n.1136T>C