Canonical Allele Identifier: CA340223218

Gene: CYP4A11

Linked Data

• COSMIC: COSM4792567
• MyVariant Identifiers: chr1:g.47398493C>G (hg19) ; chr1:g.46932821C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932821C>G , CM000663.2:g.46932821C>G	GRCh38
NC_000001.10:g.47398493C>G , CM000663.1:g.47398493C>G	GRCh37
NC_000001.9:g.47171080C>G	NCBI36
NG_007932.1:g.13664G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1304G>C MANE Select	ENSP00000311095.4:p.Arg435Pro
ENST00000310638.8:c.1304G>C	ENSP00000311095.4:p.Arg435Pro
ENST00000371904.8:c.1307G>C	ENSP00000360971.4:p.Arg436Pro
ENST00000371905.1:c.1304G>C	ENSP00000360972.1:p.Arg435Pro
ENST00000462347.5:c.1010G>C	ENSP00000477495.1:p.Arg337Pro
ENST00000465874.5:c.*102G>C	ENSP00000476368.1:n.*102G>C
ENST00000468629.5:c.*9G>C	ENSP00000476619.1:n.*9G>C
ENST00000474458.5:c.*9G>C	ENSP00000476988.1:n.*9G>C
ENST00000475477.5:c.*98G>C	ENSP00000476854.1:n.*98G>C
NM_000778.3:c.1304G>C	NP_000769.2:p.Arg435Pro
XM_005270539.1:c.1010G>C	XP_005270596.1:p.Arg337Pro
XM_011540826.1:c.1322G>C	XP_011539128.1:p.Arg441Pro
XM_011540827.1:c.1028G>C	XP_011539129.1:p.Arg343Pro
XM_011540828.1:c.1010G>C	XP_011539130.1:p.Arg337Pro
XR_246241.1:n.1208G>C
XR_246242.1:n.1192G>C
NM_001319155.1:c.1208G>C	NP_001306084.1:p.Arg403Pro
NM_001363587.1:c.1010G>C	NP_001350516.1:p.Arg337Pro
NR_134988.1:n.1009G>C
NR_134989.1:n.1200G>C
NR_134990.1:n.1194G>C
NR_134991.1:n.1181G>C
NR_134992.1:n.810G>C
NR_134993.1:n.944G>C
NR_134994.1:n.1216G>C
XM_017000465.1:c.992G>C	XP_016855954.1:p.Arg331Pro
XR_001737005.1:n.1282G>C
NM_000778.4:c.1304G>C MANE Select	NP_000769.2:p.Arg435Pro
NM_001319155.2:c.1208G>C	NP_001306084.1:p.Arg403Pro
NM_001363587.2:c.1010G>C	NP_001350516.1:p.Arg337Pro
NR_134988.2:n.1001G>C
NR_134989.2:n.1192G>C
NR_134990.2:n.1186G>C
NR_134991.2:n.1173G>C
NR_134992.2:n.802G>C
NR_134993.2:n.936G>C
NR_134994.2:n.1208G>C