Canonical Allele Identifier: CA2144024760

Gene: ZFYVE26

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67776187_67776188delinsGA , CM000676.2:g.67776187_67776188delinsGA	GRCh38
NC_000014.8:g.68242904_68242905delinsGA , CM000676.1:g.68242904_68242905delinsGA	GRCh37
NC_000014.7:g.67312657_67312658delinsGA	NCBI36
NG_011836.1:g.45402_45403delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347230.9:c.4975-82_4975-81delinsTC MANE Select	ENSP00000251119.5:n.4975-82_4975-81delinsTC
ENST00000676512.1:c.4975-82_4975-81delinsTC	ENSP00000504552.1:n.4975-82_4975-81delinsTC
ENST00000676620.1:c.4975-160_4975-159delinsTC	ENSP00000504587.1:n.4975-160_4975-159delinsTC
ENST00000678386.1:c.5020-82_5020-81delinsTC	ENSP00000503677.1:n.5020-82_5020-81delinsTC
ENST00000347230.8:c.4975-82_4975-81delinsTC	ENSP00000251119.5:n.4975-82_4975-81delinsTC
ENST00000554523.5:n.5112-82_5112-81delinsTC
ENST00000554557.5:c.*2953-82_*2953-81delinsTC	ENSP00000450431.1:n.*2953-82_*2953-81delinsTC
ENST00000555452.1:c.4975-82_4975-81delinsTC	ENSP00000450603.1:n.4975-82_4975-81delinsTC
NM_015346.3:c.4975-82_4975-81delinsTC	NP_056161.2:n.4975-82_4975-81delinsTC
XM_006720093.2:c.4975-82_4975-81delinsTC	XP_006720156.1:n.4975-82_4975-81delinsTC
XM_011536606.1:c.3466-82_3466-81delinsTC	XP_011534908.1:n.3466-82_3466-81delinsTC
XM_011536607.1:c.2650-82_2650-81delinsTC	XP_011534909.1:n.2650-82_2650-81delinsTC
XM_011536608.1:c.2557-82_2557-81delinsTC	XP_011534910.1:n.2557-82_2557-81delinsTC
XM_011536609.1:c.4975-65_4975-64delinsTC	XP_011534911.1:n.4975-65_4975-64delinsTC
XM_011536609.2:c.4975-65_4975-64delinsTC	XP_011534911.1:n.4975-65_4975-64delinsTC
XM_017021124.1:c.4975-82_4975-81delinsTC	XP_016876613.1:n.4975-82_4975-81delinsTC
XM_017021125.1:c.4975-82_4975-81delinsTC	XP_016876614.1:n.4975-82_4975-81delinsTC
XM_017021126.1:c.3466-82_3466-81delinsTC	XP_016876615.1:n.3466-82_3466-81delinsTC
XM_017021127.2:c.2650-82_2650-81delinsTC	XP_016876616.1:n.2650-82_2650-81delinsTC
XM_017021128.1:c.2557-82_2557-81delinsTC	XP_016876617.1:n.2557-82_2557-81delinsTC
NM_015346.4:c.4975-82_4975-81delinsTC MANE Select	NP_056161.2:n.4975-82_4975-81delinsTC