Canonical Allele Identifier: CA2579219775
Gene: YWHAZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.100920807_100920808insCC , CM000670.2:g.100920807_100920808insCC GRCh38
NC_000008.10:g.101933035_101933036insCC , CM000670.1:g.101933035_101933036insCC GRCh37
NC_000008.9:g.102002211_102002212insCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395958.6:c.679-56_679-55insGG MANE Select ENSP00000379288.2:n.679-56_679-55insGG
ENST00000353245.7:c.679-56_679-55insGG ENSP00000309503.3:n.679-56_679-55insGG
ENST00000395948.6:c.448-56_448-55insGG ENSP00000379278.2:n.448-56_448-55insGG
ENST00000395951.7:c.679-56_679-55insGG ENSP00000379281.3:n.679-56_679-55insGG
ENST00000395953.6:c.679-56_679-55insGG ENSP00000379283.2:n.679-56_679-55insGG
ENST00000395956.7:c.679-56_679-55insGG ENSP00000379286.3:n.679-56_679-55insGG
ENST00000395957.6:c.679-56_679-55insGG ENSP00000379287.2:n.679-56_679-55insGG
ENST00000395958.5:c.679-56_679-55insGG ENSP00000379288.2:n.679-56_679-55insGG
ENST00000419477.6:c.679-56_679-55insGG ENSP00000395114.2:n.679-56_679-55insGG
ENST00000457309.2:c.679-56_679-55insGG ENSP00000398599.1:n.679-56_679-55insGG
ENST00000521309.5:c.319-56_319-55insGG ENSP00000429623.1:n.319-56_319-55insGG
ENST00000521607.5:c.703-56_703-55insGG ENSP00000430058.1:n.703-56_703-55insGG
ENST00000522542.5:c.454-56_454-55insGG ENSP00000430072.1:n.454-56_454-55insGG
ENST00000522819.5:c.319-56_319-55insGG ENSP00000428775.1:n.319-56_319-55insGG
ENST00000523848.5:c.334-56_334-55insGG ENSP00000428860.1:n.334-56_334-55insGG
NM_001135699.1:c.679-56_679-55insGG NP_001129171.1:n.679-56_679-55insGG
NM_001135700.1:c.679-56_679-55insGG NP_001129172.1:n.679-56_679-55insGG
NM_001135701.1:c.679-56_679-55insGG NP_001129173.1:n.679-56_679-55insGG
NM_001135702.1:c.679-56_679-55insGG NP_001129174.1:n.679-56_679-55insGG
NM_003406.3:c.679-56_679-55insGG NP_003397.1:n.679-56_679-55insGG
NM_145690.2:c.679-56_679-55insGG NP_663723.1:n.679-56_679-55insGG
XM_005251061.2:c.679-56_679-55insGG XP_005251118.1:n.679-56_679-55insGG
XM_005251062.2:c.679-56_679-55insGG XP_005251119.1:n.679-56_679-55insGG
XM_005251063.2:c.679-56_679-55insGG XP_005251120.1:n.679-56_679-55insGG
XM_011517289.1:c.679-56_679-55insGG XP_011515591.1:n.679-56_679-55insGG
XM_005251061.3:c.679-56_679-55insGG XP_005251118.1:n.679-56_679-55insGG
XM_005251063.3:c.679-56_679-55insGG XP_005251120.1:n.679-56_679-55insGG
XM_017013810.2:c.679-56_679-55insGG XP_016869299.1:n.679-56_679-55insGG
XM_017013811.1:c.679-56_679-55insGG XP_016869300.1:n.679-56_679-55insGG
XM_024447266.1:c.679-56_679-55insGG XP_024303034.1:n.679-56_679-55insGG
NM_145690.3:c.679-56_679-55insGG MANE Select NP_663723.1:n.679-56_679-55insGG
NM_001135700.2:c.679-56_679-55insGG NP_001129172.1:n.679-56_679-55insGG
NM_001135701.2:c.679-56_679-55insGG NP_001129173.1:n.679-56_679-55insGG
NM_001135702.2:c.679-56_679-55insGG NP_001129174.1:n.679-56_679-55insGG
NM_003406.4:c.679-56_679-55insGG NP_003397.1:n.679-56_679-55insGG
NM_001135699.2:c.679-56_679-55insGG NP_001129171.1:n.679-56_679-55insGG