Canonical Allele Identifier: CA390168578

Gene: ZFYVE26

Linked Data

• MyVariant Identifiers: chr14:g.68242821A>C (hg19) ; chr14:g.67776104A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67776104A>C , CM000676.2:g.67776104A>C	GRCh38
NC_000014.8:g.68242821A>C , CM000676.1:g.68242821A>C	GRCh37
NC_000014.7:g.67312574A>C	NCBI36
NG_011836.1:g.45486T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4977T>G MANE Select	ENSP00000251119.5:p.Ile1659Met
ENST00000676512.1:c.4977T>G	ENSP00000504552.1:p.Ile1659Met
ENST00000676620.1:c.4975-76T>G	ENSP00000504587.1:n.4975-76T>G
ENST00000678386.1:c.5022T>G	ENSP00000503677.1:p.Ile1674Met
ENST00000347230.8:c.4977T>G	ENSP00000251119.5:p.Ile1659Met
ENST00000554523.5:n.5114T>G
ENST00000554557.5:c.*2955T>G	ENSP00000450431.1:n.*2955T>G
ENST00000555452.1:c.4977T>G	ENSP00000450603.1:p.Ile1659Met
NM_015346.3:c.4977T>G	NP_056161.2:p.Ile1659Met
XM_006720093.2:c.4977T>G	XP_006720156.1:p.Ile1659Met
XM_011536606.1:c.3468T>G	XP_011534908.1:p.Ile1156Met
XM_011536607.1:c.2652T>G	XP_011534909.1:p.Ile884Met
XM_011536608.1:c.2559T>G	XP_011534910.1:p.Ile853Met
XM_011536609.1:c.4994T>G	XP_011534911.1:p.Phe1665Cys
XM_011536609.2:c.4994T>G	XP_011534911.1:p.Phe1665Cys
XM_017021124.1:c.4977T>G	XP_016876613.1:p.Ile1659Met
XM_017021125.1:c.4977T>G	XP_016876614.1:p.Ile1659Met
XM_017021126.1:c.3468T>G	XP_016876615.1:p.Ile1156Met
XM_017021127.2:c.2652T>G	XP_016876616.1:p.Ile884Met
XM_017021128.1:c.2559T>G	XP_016876617.1:p.Ile853Met
NM_015346.4:c.4977T>G MANE Select	NP_056161.2:p.Ile1659Met