Canonical Allele Identifier: CA7239307
Community Standard Title: NM_015346.4(ZFYVE26):c.6144C>A (p.Tyr2048Ter)
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67762687G>T , CM000676.2:g.67762687G>T GRCh38
NC_000014.8:g.68229404G>T , CM000676.1:g.68229404G>T GRCh37
NC_000014.7:g.67299157G>T NCBI36
NG_011836.1:g.58903C>A

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.6144C>A MANE Select NP_056161.2:p.Tyr2048Ter
ENST00000347230.9:c.6144C>A MANE Select ENSP00000251119.5:p.Tyr2048Ter
NM_015346.3:c.6144C>A NP_056161.2:p.Tyr2048Ter
ENST00000347230.8:c.6144C>A ENSP00000251119.5:p.Tyr2048Ter
ENST00000394455.6:n.1407C>A
ENST00000554523.5:n.6281C>A
ENST00000554557.5:c.*4122C>A ENSP00000450431.1:n.*4122C>A
ENST00000555452.1:c.6144C>A ENSP00000450603.1:p.Tyr2048Ter
ENST00000676512.1:c.6162C>A ENSP00000504552.1:p.Tyr2054Ter
ENST00000676620.1:c.6066C>A ENSP00000504587.1:p.Tyr2022Ter
ENST00000678386.1:c.6189C>A ENSP00000503677.1:p.Tyr2063Ter
XM_006720093.2:c.6144C>A XP_006720156.1:p.Tyr2048Ter
XM_011536606.1:c.4635C>A XP_011534908.1:p.Tyr1545Ter
XM_011536607.1:c.3819C>A XP_011534909.1:p.Tyr1273Ter
XM_011536608.1:c.3726C>A XP_011534910.1:p.Tyr1242Ter
XM_017021124.1:c.6162C>A XP_016876613.1:p.Tyr2054Ter
XM_017021125.1:c.6162C>A XP_016876614.1:p.Tyr2054Ter
XM_017021126.1:c.4653C>A XP_016876615.1:p.Tyr1551Ter
XM_017021127.2:c.3837C>A XP_016876616.1:p.Tyr1279Ter
XM_017021128.1:c.3744C>A XP_016876617.1:p.Tyr1248Ter