Canonical Allele Identifier: CA391768346

Gene: ZFYVE19

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40813728T>A , CM000677.2:g.40813728T>A	GRCh38
NC_000015.9:g.41105926T>A , CM000677.1:g.41105926T>A	GRCh37
NC_000015.8:g.38893218T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299173.14:c.922T>A	ENSP00000299173.10:p.Ser308Thr
ENST00000336455.9:c.1096T>A	ENSP00000337824.5:p.Ser366Thr
ENST00000355341.8:c.1126T>A MANE Select	ENSP00000347498.4:p.Ser376Thr
ENST00000560078.1:n.2203T>A
ENST00000561768.5:c.901T>A
ENST00000563497.1:n.66T>A
ENST00000564258.5:c.601T>A	ENSP00000457617.1:p.Ser201Thr
ENST00000566407.5:c.850T>A	ENSP00000456304.1:p.Ser284Thr
ENST00000569057.5:c.831T>A
ENST00000570108.5:c.1057T>A	ENSP00000456223.1:p.Ser353Thr
NM_001077268.1:c.1126T>A	NP_001070736.1:p.Ser376Thr
NM_001258420.1:c.922T>A	NP_001245349.1:p.Ser308Thr
NM_001258421.1:c.601T>A	NP_001245350.1:p.Ser201Thr
NM_032850.4:c.1096T>A	NP_116239.3:p.Ser366Thr
XM_024450092.1:c.469T>A	XP_024305860.1:p.Ser157Thr
NM_001077268.2:c.1126T>A MANE Select	NP_001070736.1:p.Ser376Thr
NM_001258420.2:c.922T>A	NP_001245349.1:p.Ser308Thr
NM_001258421.2:c.601T>A	NP_001245350.1:p.Ser201Thr
NM_032850.5:c.1096T>A	NP_116239.3:p.Ser366Thr