Canonical Allele Identifier: CA7239208

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67761414G>A , CM000676.2:g.67761414G>A	GRCh38
NC_000014.8:g.68228131G>A , CM000676.1:g.68228131G>A	GRCh37
NC_000014.7:g.67297884G>A	NCBI36
NG_011836.1:g.60176C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6540C>T MANE Select	NP_056161.2:p.Tyr2180=
ENST00000347230.9:c.6540C>T MANE Select	ENSP00000251119.5:p.Tyr2180=
NM_015346.3:c.6540C>T	NP_056161.2:p.Tyr2180=
ENST00000347230.8:c.6540C>T	ENSP00000251119.5:p.Tyr2180=
ENST00000394455.6:n.1803C>T
ENST00000554523.5:n.7295C>T
ENST00000554557.5:c.*4518C>T	ENSP00000450431.1:n.*4518C>T
ENST00000555452.1:c.6540C>T	ENSP00000450603.1:p.Tyr2180=
ENST00000557306.1:c.78C>T	ENSP00000452142.1:p.Tyr26=
ENST00000676512.1:c.6558C>T	ENSP00000504552.1:p.Tyr2186=
ENST00000676620.1:c.6462C>T	ENSP00000504587.1:p.Tyr2154=
ENST00000678386.1:c.6585C>T	ENSP00000503677.1:p.Tyr2195=
XM_006720093.2:c.6540C>T	XP_006720156.1:p.Tyr2180=
XM_011536606.1:c.5031C>T	XP_011534908.1:p.Tyr1677=
XM_011536607.1:c.4215C>T	XP_011534909.1:p.Tyr1405=
XM_011536608.1:c.4122C>T	XP_011534910.1:p.Tyr1374=
XM_017021124.1:c.6558C>T	XP_016876613.1:p.Tyr2186=
XM_017021125.1:c.6558C>T	XP_016876614.1:p.Tyr2186=
XM_017021126.1:c.5049C>T	XP_016876615.1:p.Tyr1683=
XM_017021127.2:c.4233C>T	XP_016876616.1:p.Tyr1411=
XM_017021128.1:c.4140C>T	XP_016876617.1:p.Tyr1380=