Canonical Allele Identifier: CA390175468

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67798291G>C , CM000676.2:g.67798291G>C	GRCh38
NC_000014.8:g.68265008G>C , CM000676.1:g.68265008G>C	GRCh37
NC_000014.7:g.67334761G>C	NCBI36
NG_011836.1:g.23299C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.1971C>G MANE Select	NP_056161.2:p.Tyr657Ter
ENST00000347230.9:c.1971C>G MANE Select	ENSP00000251119.5:p.Tyr657Ter
NM_015346.3:c.1971C>G	NP_056161.2:p.Tyr657Ter
ENST00000347230.8:c.1971C>G	ENSP00000251119.5:p.Tyr657Ter
ENST00000554523.5:n.2108C>G
ENST00000554557.5:c.*268C>G	ENSP00000450431.1:n.*268C>G
ENST00000555452.1:c.1971C>G	ENSP00000450603.1:p.Tyr657Ter
ENST00000557366.5:n.2017C>G
ENST00000557407.1:n.2106C>G
ENST00000676512.1:c.1971C>G	ENSP00000504552.1:p.Tyr657Ter
ENST00000676620.1:c.1971C>G	ENSP00000504587.1:p.Tyr657Ter
ENST00000677026.1:c.1767C>G	ENSP00000503710.1:p.Tyr589Ter
ENST00000678382.1:c.*966C>G	ENSP00000504130.1:n.*966C>G
ENST00000678386.1:c.1971C>G	ENSP00000503677.1:p.Tyr657Ter
XM_006720093.2:c.1971C>G	XP_006720156.1:p.Tyr657Ter
XM_011536606.1:c.462C>G	XP_011534908.1:p.Tyr154Ter
XM_011536609.1:c.1971C>G	XP_011534911.1:p.Tyr657Ter
XM_011536609.2:c.1971C>G	XP_011534911.1:p.Tyr657Ter
XM_017021124.1:c.1971C>G	XP_016876613.1:p.Tyr657Ter
XM_017021125.1:c.1971C>G	XP_016876614.1:p.Tyr657Ter
XM_017021126.1:c.462C>G	XP_016876615.1:p.Tyr154Ter