Canonical Allele Identifier: CA340223100

Gene: CYP4A11

Linked Data

• MyVariant Identifiers: chr1:g.47398436G>C (hg19) ; chr1:g.46932764G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932764G>C , CM000663.2:g.46932764G>C	GRCh38
NC_000001.10:g.47398436G>C , CM000663.1:g.47398436G>C	GRCh37
NC_000001.9:g.47171023G>C	NCBI36
NG_007932.1:g.13721C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310638.9:c.1361C>G MANE Select	ENSP00000311095.4:p.Ser454Ter
ENST00000310638.8:c.1361C>G	ENSP00000311095.4:p.Ser454Ter
ENST00000371904.8:c.1364C>G	ENSP00000360971.4:p.Ser455Ter
ENST00000371905.1:c.1361C>G	ENSP00000360972.1:p.Ser454Ter
ENST00000462347.5:c.1067C>G	ENSP00000477495.1:p.Ser356Ter
ENST00000465874.5:c.*159C>G	ENSP00000476368.1:n.*159C>G
ENST00000468629.5:c.*66C>G	ENSP00000476619.1:n.*66C>G
ENST00000474458.5:c.*66C>G	ENSP00000476988.1:n.*66C>G
ENST00000475477.5:c.*155C>G	ENSP00000476854.1:n.*155C>G
NM_000778.3:c.1361C>G	NP_000769.2:p.Ser454Ter
XM_005270539.1:c.1067C>G	XP_005270596.1:p.Ser356Ter
XM_011540826.1:c.1379C>G	XP_011539128.1:p.Ser460Ter
XM_011540827.1:c.1085C>G	XP_011539129.1:p.Ser362Ter
XM_011540828.1:c.1067C>G	XP_011539130.1:p.Ser356Ter
XR_246241.1:n.1265C>G
XR_246242.1:n.1249C>G
NM_001319155.1:c.1265C>G	NP_001306084.1:p.Ser422Ter
NM_001363587.1:c.1067C>G	NP_001350516.1:p.Ser356Ter
NR_134988.1:n.1066C>G
NR_134989.1:n.1257C>G
NR_134990.1:n.1251C>G
NR_134991.1:n.1238C>G
NR_134992.1:n.867C>G
NR_134993.1:n.1001C>G
NR_134994.1:n.1273C>G
XM_017000465.1:c.1049C>G	XP_016855954.1:p.Ser350Ter
XR_001737005.1:n.1339C>G
NM_000778.4:c.1361C>G MANE Select	NP_000769.2:p.Ser454Ter
NM_001319155.2:c.1265C>G	NP_001306084.1:p.Ser422Ter
NM_001363587.2:c.1067C>G	NP_001350516.1:p.Ser356Ter
NR_134988.2:n.1058C>G
NR_134989.2:n.1249C>G
NR_134990.2:n.1243C>G
NR_134991.2:n.1230C>G
NR_134992.2:n.859C>G
NR_134993.2:n.993C>G
NR_134994.2:n.1265C>G