Canonical Allele Identifier: CA340223278

Gene: CYP4A11

Linked Data

• COSMIC: COSM4451550
• MyVariant Identifiers: chr1:g.47398662T>C (hg19) ; chr1:g.46932990T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46932990T>C , CM000663.2:g.46932990T>C	GRCh38
NC_000001.10:g.47398662T>C , CM000663.1:g.47398662T>C	GRCh37
NC_000001.9:g.47171249T>C	NCBI36
NG_007932.1:g.13495A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310638.9:c.1280A>G MANE Select	ENSP00000311095.4:p.Asn427Ser
ENST00000310638.8:c.1280A>G	ENSP00000311095.4:p.Asn427Ser
ENST00000371904.8:c.1283A>G	ENSP00000360971.4:p.Asn428Ser
ENST00000371905.1:c.1280A>G	ENSP00000360972.1:p.Asn427Ser
ENST00000462347.5:c.986A>G	ENSP00000477495.1:p.Asn329Ser
ENST00000465874.5:c.*78A>G	ENSP00000476368.1:n.*78A>G
ENST00000468629.5:c.1127-153A>G	ENSP00000476619.1:n.1127-153A>G
ENST00000474458.5:c.743-153A>G	ENSP00000476988.1:n.743-153A>G
ENST00000475477.5:c.*82-153A>G	ENSP00000476854.1:n.*82-153A>G
NM_000778.3:c.1280A>G	NP_000769.2:p.Asn427Ser
XM_005270539.1:c.986A>G	XP_005270596.1:p.Asn329Ser
XM_011540826.1:c.1298A>G	XP_011539128.1:p.Asn433Ser
XM_011540827.1:c.1004A>G	XP_011539129.1:p.Asn335Ser
XM_011540828.1:c.986A>G	XP_011539130.1:p.Asn329Ser
XR_246241.1:n.1184A>G
XR_246242.1:n.1168A>G
NM_001319155.1:c.1184A>G	NP_001306084.1:p.Asn395Ser
NM_001363587.1:c.986A>G	NP_001350516.1:p.Asn329Ser
NR_134988.1:n.985A>G
NR_134989.1:n.1176A>G
NR_134990.1:n.1178-153A>G
NR_134991.1:n.1157A>G
NR_134992.1:n.794-153A>G
NR_134993.1:n.928-153A>G
NR_134994.1:n.1192A>G
XM_017000465.1:c.968A>G	XP_016855954.1:p.Asn323Ser
XR_001737005.1:n.1266-153A>G
NM_000778.4:c.1280A>G MANE Select	NP_000769.2:p.Asn427Ser
NM_001319155.2:c.1184A>G	NP_001306084.1:p.Asn395Ser
NM_001363587.2:c.986A>G	NP_001350516.1:p.Asn329Ser
NR_134988.2:n.977A>G
NR_134989.2:n.1168A>G
NR_134990.2:n.1170-153A>G
NR_134991.2:n.1149A>G
NR_134992.2:n.786-153A>G
NR_134993.2:n.920-153A>G
NR_134994.2:n.1184A>G