Canonical Allele Identifier: CA7239119

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67755161T>C , CM000676.2:g.67755161T>C	GRCh38
NC_000014.8:g.68221878T>C , CM000676.1:g.68221878T>C	GRCh37
NC_000014.7:g.67291631T>C	NCBI36
NG_011836.1:g.66429A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.6876A>G MANE Select	NP_056161.2:p.Leu2292=
ENST00000347230.9:c.6876A>G MANE Select	ENSP00000251119.5:p.Leu2292=
NM_015346.3:c.6876A>G	NP_056161.2:p.Leu2292=
ENST00000347230.8:c.6876A>G	ENSP00000251119.5:p.Leu2292=
ENST00000394455.6:n.2139A>G
ENST00000554523.5:n.7631A>G
ENST00000554557.5:c.*4854A>G	ENSP00000450431.1:n.*4854A>G
ENST00000554783.1:n.564A>G
ENST00000557306.1:c.414A>G	ENSP00000452142.1:p.Leu138=
ENST00000676512.1:c.6894A>G	ENSP00000504552.1:p.Leu2298=
ENST00000676620.1:c.6798A>G	ENSP00000504587.1:p.Leu2266=
ENST00000678386.1:c.6921A>G	ENSP00000503677.1:p.Leu2307=
XM_006720093.2:c.6876A>G	XP_006720156.1:p.Leu2292=
XM_011536606.1:c.5367A>G	XP_011534908.1:p.Leu1789=
XM_011536607.1:c.4551A>G	XP_011534909.1:p.Leu1517=
XM_011536608.1:c.4458A>G	XP_011534910.1:p.Leu1486=
XM_017021124.1:c.6894A>G	XP_016876613.1:p.Leu2298=
XM_017021125.1:c.6894A>G	XP_016876614.1:p.Leu2298=
XM_017021126.1:c.5385A>G	XP_016876615.1:p.Leu1795=
XM_017021127.2:c.4569A>G	XP_016876616.1:p.Leu1523=
XM_017021128.1:c.4476A>G	XP_016876617.1:p.Leu1492=