Canonical Allele Identifier: CA7485412

Gene: ZFYVE19

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40807615C>G , CM000677.2:g.40807615C>G	GRCh38
NC_000015.9:g.41099813C>G , CM000677.1:g.41099813C>G	GRCh37
NC_000015.8:g.38887105C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001077268.2:c.26C>G MANE Select	NP_001070736.1:p.Pro9Arg
ENST00000355341.8:c.26C>G MANE Select	ENSP00000347498.4:p.Pro9Arg
NM_001077268.1:c.26C>G	NP_001070736.1:p.Pro9Arg
NM_001258420.1:c.26C>G	NP_001245349.1:p.Pro9Arg
NM_001258420.2:c.26C>G	NP_001245349.1:p.Pro9Arg
NM_001258421.1:c.-303C>G	NP_001245350.1:n.-303C>G
NM_001258421.2:c.-303C>G	NP_001245350.1:n.-303C>G
NM_032850.4:c.125+202C>G	NP_116239.3:n.125+202C>G
NM_032850.5:c.125+202C>G	NP_116239.3:n.125+202C>G
ENST00000299173.14:c.26C>G	ENSP00000299173.10:p.Pro9Arg
ENST00000336455.9:c.125+202C>G	ENSP00000337824.5:n.125+202C>G
ENST00000564258.5:c.-303C>G	ENSP00000457617.1:n.-303C>G
ENST00000570108.5:c.134-177C>G	ENSP00000456223.1:n.134-177C>G
XM_017022684.2:c.26C>G	XP_016878173.1:p.Pro9Arg
XR_931925.1:n.540C>G
XR_931925.3:n.530C>G