Canonical Allele Identifier: CA340223386

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398714T>C (hg19) ; chr1:g.46933042T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46933042T>C , CM000663.2:g.46933042T>C	GRCh38
NC_000001.10:g.47398714T>C , CM000663.1:g.47398714T>C	GRCh37
NC_000001.9:g.47171301T>C	NCBI36
NG_007932.1:g.13443A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1228A>G MANE Select	ENSP00000311095.4:p.Met410Val
ENST00000310638.8:c.1228A>G	ENSP00000311095.4:p.Met410Val
ENST00000371904.8:c.1231A>G	ENSP00000360971.4:p.Met411Val
ENST00000371905.1:c.1228A>G	ENSP00000360972.1:p.Met410Val
ENST00000462347.5:c.934A>G	ENSP00000477495.1:p.Met312Val
ENST00000465874.5:c.*26A>G	ENSP00000476368.1:n.*26A>G
ENST00000468629.5:c.1127-205A>G	ENSP00000476619.1:n.1127-205A>G
ENST00000474458.5:c.743-205A>G	ENSP00000476988.1:n.743-205A>G
ENST00000475477.5:c.*82-205A>G	ENSP00000476854.1:n.*82-205A>G
NM_000778.3:c.1228A>G	NP_000769.2:p.Met410Val
XM_005270539.1:c.934A>G	XP_005270596.1:p.Met312Val
XM_011540826.1:c.1246A>G	XP_011539128.1:p.Met416Val
XM_011540827.1:c.952A>G	XP_011539129.1:p.Met318Val
XM_011540828.1:c.934A>G	XP_011539130.1:p.Met312Val
XR_246241.1:n.1132A>G
XR_246242.1:n.1116A>G
NM_001319155.1:c.1132A>G	NP_001306084.1:p.Met378Val
NM_001363587.1:c.934A>G	NP_001350516.1:p.Met312Val
NR_134988.1:n.933A>G
NR_134989.1:n.1124A>G
NR_134990.1:n.1178-205A>G
NR_134991.1:n.1105A>G
NR_134992.1:n.794-205A>G
NR_134993.1:n.928-205A>G
NR_134994.1:n.1140A>G
XM_017000465.1:c.916A>G	XP_016855954.1:p.Met306Val
XR_001737005.1:n.1266-205A>G
NM_000778.4:c.1228A>G MANE Select	NP_000769.2:p.Met410Val
NM_001319155.2:c.1132A>G	NP_001306084.1:p.Met378Val
NM_001363587.2:c.934A>G	NP_001350516.1:p.Met312Val
NR_134988.2:n.925A>G
NR_134989.2:n.1116A>G
NR_134990.2:n.1170-205A>G
NR_134991.2:n.1097A>G
NR_134992.2:n.786-205A>G
NR_134993.2:n.920-205A>G
NR_134994.2:n.1132A>G