Canonical Allele Identifier: CA362212764

Gene: FBXW11

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171869770G>C , CM000667.2:g.171869770G>C	GRCh38
NC_000005.9:g.171296774G>C , CM000667.1:g.171296774G>C	GRCh37
NC_000005.8:g.171229379G>C	NCBI36
NG_009275.1:g.142104C>G
NG_009275.2:g.142104C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378974.1:c.1489C>G MANE Select	NP_001365903.1:p.Pro497Ala
ENST00000517395.6:c.1489C>G MANE Select	ENSP00000428753.2:p.Pro497Ala
NM_001378975.1:c.1420C>G	NP_001365904.1:p.Pro474Ala
NM_001378976.1:c.1393C>G	NP_001365905.1:p.Pro465Ala
NM_001378977.1:c.1330C>G	NP_001365906.1:p.Pro444Ala
NM_001378978.1:c.1330C>G	NP_001365907.1:p.Pro444Ala
NM_001378979.1:c.1330C>G	NP_001365908.1:p.Pro444Ala
NM_001378980.1:c.1324C>G	NP_001365909.1:p.Pro442Ala
NM_012300.2:c.1426C>G	NP_036432.2:p.Pro476Ala
NM_012300.3:c.1426C>G	NP_036432.2:p.Pro476Ala
NM_033644.2:c.1387C>G	NP_387448.2:p.Pro463Ala
NM_033644.3:c.1387C>G	NP_387448.2:p.Pro463Ala
NM_033645.2:c.1324C>G	NP_387449.2:p.Pro442Ala
NM_033645.3:c.1324C>G	NP_387449.2:p.Pro442Ala
ENST00000265094.9:c.1426C>G	ENSP00000265094.5:p.Pro476Ala
ENST00000296933.10:c.1387C>G	ENSP00000296933.6:p.Pro463Ala
ENST00000393802.6:c.1324C>G	ENSP00000377391.2:p.Pro442Ala
ENST00000522376.1:n.275C>G
ENST00000523843.5:c.*1405C>G	ENSP00000430104.1:n.*1405C>G
XM_005265855.3:c.1489C>G	XP_005265912.1:p.Pro497Ala
XM_005265855.5:c.1489C>G	XP_005265912.1:p.Pro497Ala
XM_005265856.1:c.1393C>G	XP_005265913.1:p.Pro465Ala
XM_005265856.2:c.1393C>G	XP_005265913.1:p.Pro465Ala
XM_005265857.2:c.1345C>G	XP_005265914.1:p.Pro449Ala
XM_005265858.1:c.1330C>G	XP_005265915.1:p.Pro444Ala
XM_005265858.3:c.1330C>G	XP_005265915.1:p.Pro444Ala
XM_011534492.1:c.1420C>G	XP_011532794.1:p.Pro474Ala
XM_017009279.1:c.1426C>G	XP_016864768.1:p.Pro476Ala
XM_017009280.2:c.1330C>G	XP_016864769.1:p.Pro444Ala
XM_017009281.2:c.1330C>G	XP_016864770.1:p.Pro444Ala