Canonical Allele Identifier: CA486970567

Gene: ZFYVE26

Linked Data

• MyVariant Identifiers: chr14:g.68242812G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67776095G>C , CM000676.2:g.67776095G>C	GRCh38
NC_000014.8:g.68242812G>C , CM000676.1:g.68242812G>C	GRCh37
NC_000014.7:g.67312565G>C	NCBI36
NG_011836.1:g.45495C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4986C>G MANE Select	ENSP00000251119.5:p.Thr1662=
ENST00000676512.1:c.4986C>G	ENSP00000504552.1:p.Thr1662=
ENST00000676620.1:c.4975-67C>G	ENSP00000504587.1:n.4975-67C>G
ENST00000678386.1:c.5031C>G	ENSP00000503677.1:p.Thr1677=
ENST00000347230.8:c.4986C>G	ENSP00000251119.5:p.Thr1662=
ENST00000554523.5:n.5123C>G
ENST00000554557.5:c.*2964C>G	ENSP00000450431.1:n.*2964C>G
ENST00000555452.1:c.4986C>G	ENSP00000450603.1:p.Thr1662=
NM_015346.3:c.4986C>G	NP_056161.2:p.Thr1662=
XM_006720093.2:c.4986C>G	XP_006720156.1:p.Thr1662=
XM_011536606.1:c.3477C>G	XP_011534908.1:p.Thr1159=
XM_011536607.1:c.2661C>G	XP_011534909.1:p.Thr887=
XM_011536608.1:c.2568C>G	XP_011534910.1:p.Thr856=
XM_011536609.1:c.*2C>G	XP_011534911.1:n.*2C>G
XM_011536609.2:c.*2C>G	XP_011534911.1:n.*2C>G
XM_017021124.1:c.4986C>G	XP_016876613.1:p.Thr1662=
XM_017021125.1:c.4986C>G	XP_016876614.1:p.Thr1662=
XM_017021126.1:c.3477C>G	XP_016876615.1:p.Thr1159=
XM_017021127.2:c.2661C>G	XP_016876616.1:p.Thr887=
XM_017021128.1:c.2568C>G	XP_016876617.1:p.Thr856=
NM_015346.4:c.4986C>G MANE Select	NP_056161.2:p.Thr1662=