Canonical Allele Identifier: CA736354385

Gene: CYP4A11

Linked Data

• dbSNP Id: rs1345089263
• MyVariant Identifiers: chr1:g.47396971T>C (hg19) ; chr1:g.46931299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46931299T>C , CM000663.2:g.46931299T>C	GRCh38
NC_000001.10:g.47396971T>C , CM000663.1:g.47396971T>C	GRCh37
NC_000001.9:g.47169558T>C	NCBI36
NG_007932.1:g.15186A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1365-989A>G MANE Select	ENSP00000311095.4:n.1365-989A>G
ENST00000310638.8:c.1365-989A>G	ENSP00000311095.4:n.1365-989A>G
ENST00000371904.8:c.1368-989A>G	ENSP00000360971.4:n.1368-989A>G
ENST00000462347.5:c.1071-989A>G	ENSP00000477495.1:n.1071-989A>G
ENST00000468629.5:c.*70-989A>G	ENSP00000476619.1:n.*70-989A>G
ENST00000474458.5:c.*70-989A>G	ENSP00000476988.1:n.*70-989A>G
ENST00000475477.5:c.*159-989A>G	ENSP00000476854.1:n.*159-989A>G
NM_000778.3:c.1365-989A>G	NP_000769.2:n.1365-989A>G
XM_011540826.1:c.1383-989A>G	XP_011539128.1:n.1383-989A>G
XM_011540827.1:c.1089-989A>G	XP_011539129.1:n.1089-989A>G
XM_011540828.1:c.1071-989A>G	XP_011539130.1:n.1071-989A>G
XR_246241.1:n.1269-989A>G
XR_246242.1:n.1253-989A>G
NM_001319155.1:c.1269-989A>G	NP_001306084.1:n.1269-989A>G
NM_001363587.1:c.1071-989A>G	NP_001350516.1:n.1071-989A>G
NR_134988.1:n.1070-989A>G
NR_134989.1:n.1261-989A>G
NR_134990.1:n.1255-989A>G
NR_134991.1:n.1242-989A>G
NR_134992.1:n.871-989A>G
NR_134993.1:n.1005-989A>G
NR_134994.1:n.1277-989A>G
XM_017000465.1:c.1053-989A>G	XP_016855954.1:n.1053-989A>G
XR_001737005.1:n.1343-989A>G
NM_000778.4:c.1365-989A>G MANE Select	NP_000769.2:n.1365-989A>G
NM_001319155.2:c.1269-989A>G	NP_001306084.1:n.1269-989A>G
NM_001363587.2:c.1071-989A>G	NP_001350516.1:n.1071-989A>G
NR_134988.2:n.1062-989A>G
NR_134989.2:n.1253-989A>G
NR_134990.2:n.1247-989A>G
NR_134991.2:n.1234-989A>G
NR_134992.2:n.863-989A>G
NR_134993.2:n.997-989A>G
NR_134994.2:n.1269-989A>G