Canonical Allele Identifier: CA7239851

Gene: ZFYVE26

Linked Data

• ClinVar Variation Id: 313901
• ClinVar RCV Id: RCV000333452 ; RCV000442507 ; RCV000860479 ; RCV001848646 ; RCV003311751
• dbSNP Id: rs374530573
• ExAC: 14:68249834 C / A
• gnomAD v2: 14-68249834-C-A
• gnomAD v3: 14-67783117-C-A
• gnomAD v4: 14-67783117-C-A
• MyVariant Identifiers: chr14:g.68249834C>A (hg19) ; chr14:g.67783117C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67783117C>A , CM000676.2:g.67783117C>A	GRCh38
NC_000014.8:g.68249834C>A , CM000676.1:g.68249834C>A	GRCh37
NC_000014.7:g.67319587C>A	NCBI36
NG_011836.1:g.38473G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4035G>T MANE Select	ENSP00000251119.5:p.Val1345=
ENST00000676512.1:c.4035G>T	ENSP00000504552.1:p.Val1345=
ENST00000676620.1:c.4035G>T	ENSP00000504587.1:p.Val1345=
ENST00000678386.1:c.4035G>T	ENSP00000503677.1:p.Val1345=
ENST00000347230.8:c.4035G>T	ENSP00000251119.5:p.Val1345=
ENST00000554523.5:n.4172G>T
ENST00000554557.5:c.*2332G>T	ENSP00000450431.1:n.*2332G>T
ENST00000555452.1:c.4035G>T	ENSP00000450603.1:p.Val1345=
NM_015346.3:c.4035G>T	NP_056161.2:p.Val1345=
XM_006720093.2:c.4035G>T	XP_006720156.1:p.Val1345=
XM_011536606.1:c.2526G>T	XP_011534908.1:p.Val842=
XM_011536607.1:c.1710G>T	XP_011534909.1:p.Val570=
XM_011536608.1:c.1617G>T	XP_011534910.1:p.Val539=
XM_011536609.1:c.4035G>T	XP_011534911.1:p.Val1345=
XM_011536609.2:c.4035G>T	XP_011534911.1:p.Val1345=
XM_017021124.1:c.4035G>T	XP_016876613.1:p.Val1345=
XM_017021125.1:c.4035G>T	XP_016876614.1:p.Val1345=
XM_017021126.1:c.2526G>T	XP_016876615.1:p.Val842=
XM_017021127.2:c.1710G>T	XP_016876616.1:p.Val570=
XM_017021128.1:c.1617G>T	XP_016876617.1:p.Val539=
NM_015346.4:c.4035G>T MANE Select	NP_056161.2:p.Val1345=