Canonical Allele Identifier: CA390170635

Gene: ZFYVE26

Linked Data

• MyVariant Identifiers: chr14:g.68249673G>C (hg19) ; chr14:g.67782956G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67782956G>C , CM000676.2:g.67782956G>C	GRCh38
NC_000014.8:g.68249673G>C , CM000676.1:g.68249673G>C	GRCh37
NC_000014.7:g.67319426G>C	NCBI36
NG_011836.1:g.38634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4196C>G MANE Select	ENSP00000251119.5:p.Thr1399Ser
ENST00000676512.1:c.4196C>G	ENSP00000504552.1:p.Thr1399Ser
ENST00000676620.1:c.4196C>G	ENSP00000504587.1:p.Thr1399Ser
ENST00000678386.1:c.4196C>G	ENSP00000503677.1:p.Thr1399Ser
ENST00000347230.8:c.4196C>G	ENSP00000251119.5:p.Thr1399Ser
ENST00000554523.5:n.4333C>G
ENST00000554557.5:c.*2350+143C>G	ENSP00000450431.1:n.*2350+143C>G
ENST00000555452.1:c.4196C>G	ENSP00000450603.1:p.Thr1399Ser
NM_015346.3:c.4196C>G	NP_056161.2:p.Thr1399Ser
XM_006720093.2:c.4196C>G	XP_006720156.1:p.Thr1399Ser
XM_011536606.1:c.2687C>G	XP_011534908.1:p.Thr896Ser
XM_011536607.1:c.1871C>G	XP_011534909.1:p.Thr624Ser
XM_011536608.1:c.1778C>G	XP_011534910.1:p.Thr593Ser
XM_011536609.1:c.4196C>G	XP_011534911.1:p.Thr1399Ser
XM_011536609.2:c.4196C>G	XP_011534911.1:p.Thr1399Ser
XM_017021124.1:c.4196C>G	XP_016876613.1:p.Thr1399Ser
XM_017021125.1:c.4196C>G	XP_016876614.1:p.Thr1399Ser
XM_017021126.1:c.2687C>G	XP_016876615.1:p.Thr896Ser
XM_017021127.2:c.1871C>G	XP_016876616.1:p.Thr624Ser
XM_017021128.1:c.1778C>G	XP_016876617.1:p.Thr593Ser
NM_015346.4:c.4196C>G MANE Select	NP_056161.2:p.Thr1399Ser