Canonical Allele Identifier: CA390160503

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67807397C>G , CM000676.2:g.67807397C>G	GRCh38
NC_000014.8:g.68274114C>G , CM000676.1:g.68274114C>G	GRCh37
NC_000014.7:g.67343867C>G	NCBI36
NG_011836.1:g.14193G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015346.4:c.886+1G>C MANE Select	NP_056161.2:n.886+1G>C
ENST00000347230.9:c.886+1G>C MANE Select	ENSP00000251119.5:n.886+1G>C
NM_015346.3:c.886+1G>C	NP_056161.2:n.886+1G>C
ENST00000347230.8:c.886+1G>C	ENSP00000251119.5:n.886+1G>C
ENST00000554523.5:n.1023+1G>C
ENST00000554557.5:c.886+1G>C	ENSP00000450431.1:n.886+1G>C
ENST00000555452.1:c.886+1G>C	ENSP00000450603.1:n.886+1G>C
ENST00000557366.5:n.1021+1G>C
ENST00000557407.1:n.1021+1G>C
ENST00000676512.1:c.886+1G>C	ENSP00000504552.1:n.886+1G>C
ENST00000676620.1:c.886+1G>C	ENSP00000504587.1:n.886+1G>C
ENST00000677026.1:c.886+1G>C	ENSP00000503710.1:n.886+1G>C
ENST00000678382.1:c.886+1G>C	ENSP00000504130.1:n.886+1G>C
ENST00000678386.1:c.886+1G>C	ENSP00000503677.1:n.886+1G>C
XM_006720093.2:c.886+1G>C	XP_006720156.1:n.886+1G>C
XM_011536606.1:c.-535+1G>C	XP_011534908.1:n.-535+1G>C
XM_011536609.1:c.886+1G>C	XP_011534911.1:n.886+1G>C
XM_011536609.2:c.886+1G>C	XP_011534911.1:n.886+1G>C
XM_017021124.1:c.886+1G>C	XP_016876613.1:n.886+1G>C
XM_017021125.1:c.886+1G>C	XP_016876614.1:n.886+1G>C
XM_017021126.1:c.-535+1G>C	XP_016876615.1:n.-535+1G>C