Canonical Allele Identifier: CA7239382
Community Standard Title: NM_015346.4(ZFYVE26):c.5791-6G>A
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67766453C>T , CM000676.2:g.67766453C>T GRCh38
NC_000014.8:g.68233170C>T , CM000676.1:g.68233170C>T GRCh37
NC_000014.7:g.67302923C>T NCBI36
NG_011836.1:g.55137G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.5791-6G>A MANE Select NP_056161.2:n.5791-6G>A
ENST00000347230.9:c.5791-6G>A MANE Select ENSP00000251119.5:n.5791-6G>A
NM_015346.3:c.5791-6G>A NP_056161.2:n.5791-6G>A
ENST00000347230.8:c.5791-6G>A ENSP00000251119.5:n.5791-6G>A
ENST00000394455.6:n.1054-6G>A
ENST00000554523.5:n.5928-6G>A
ENST00000554557.5:c.*3769-6G>A ENSP00000450431.1:n.*3769-6G>A
ENST00000555452.1:c.5791-6G>A ENSP00000450603.1:n.5791-6G>A
ENST00000676512.1:c.5809-6G>A ENSP00000504552.1:n.5809-6G>A
ENST00000676620.1:c.5713-6G>A ENSP00000504587.1:n.5713-6G>A
ENST00000678386.1:c.5836-6G>A ENSP00000503677.1:n.5836-6G>A
XM_006720093.2:c.5791-6G>A XP_006720156.1:n.5791-6G>A
XM_011536606.1:c.4282-6G>A XP_011534908.1:n.4282-6G>A
XM_011536607.1:c.3466-6G>A XP_011534909.1:n.3466-6G>A
XM_011536608.1:c.3373-6G>A XP_011534910.1:n.3373-6G>A
XM_017021124.1:c.5809-6G>A XP_016876613.1:n.5809-6G>A
XM_017021125.1:c.5809-6G>A XP_016876614.1:n.5809-6G>A
XM_017021126.1:c.4300-6G>A XP_016876615.1:n.4300-6G>A
XM_017021127.2:c.3484-6G>A XP_016876616.1:n.3484-6G>A
XM_017021128.1:c.3391-6G>A XP_016876617.1:n.3391-6G>A