Canonical Allele Identifier: CA486971215
Community Standard Title: NM_015346.4(ZFYVE26):c.1944T>C (p.His648=)
Gene: ZFYVE26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67798318A>G , CM000676.2:g.67798318A>G GRCh38
NC_000014.8:g.68265035A>G , CM000676.1:g.68265035A>G GRCh37
NC_000014.7:g.67334788A>G NCBI36
NG_011836.1:g.23272T>C

Transcript Alleles

HGVS Amino-acid Change
NM_015346.4:c.1944T>C MANE Select NP_056161.2:p.His648=
ENST00000347230.9:c.1944T>C MANE Select ENSP00000251119.5:p.His648=
NM_015346.3:c.1944T>C NP_056161.2:p.His648=
ENST00000347230.8:c.1944T>C ENSP00000251119.5:p.His648=
ENST00000554523.5:n.2081T>C
ENST00000554557.5:c.*241T>C ENSP00000450431.1:n.*241T>C
ENST00000555452.1:c.1944T>C ENSP00000450603.1:p.His648=
ENST00000557366.5:n.1990T>C
ENST00000557407.1:n.2079T>C
ENST00000676512.1:c.1944T>C ENSP00000504552.1:p.His648=
ENST00000676620.1:c.1944T>C ENSP00000504587.1:p.His648=
ENST00000677026.1:c.1740T>C ENSP00000503710.1:p.His580=
ENST00000678382.1:c.*939T>C ENSP00000504130.1:n.*939T>C
ENST00000678386.1:c.1944T>C ENSP00000503677.1:p.His648=
XM_006720093.2:c.1944T>C XP_006720156.1:p.His648=
XM_011536606.1:c.435T>C XP_011534908.1:p.His145=
XM_011536609.1:c.1944T>C XP_011534911.1:p.His648=
XM_011536609.2:c.1944T>C XP_011534911.1:p.His648=
XM_017021124.1:c.1944T>C XP_016876613.1:p.His648=
XM_017021125.1:c.1944T>C XP_016876614.1:p.His648=
XM_017021126.1:c.435T>C XP_016876615.1:p.His145=