Canonical Allele Identifier: CA1117190232

Gene: YWHAZ

Linked Data

• gnomAD v3: 8-100920810-GTT-G
• gnomAD v4: 8-100920810-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100920813_100920814del , CM000670.2:g.100920813_100920814del	GRCh38
NC_000008.10:g.101933041_101933042del , CM000670.1:g.101933041_101933042del	GRCh37
NC_000008.9:g.102002217_102002218del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395958.6:c.679-60_679-59del MANE Select	ENSP00000379288.2:n.679-60_679-59del
ENST00000353245.7:c.679-60_679-59del	ENSP00000309503.3:n.679-60_679-59del
ENST00000395948.6:c.448-60_448-59del	ENSP00000379278.2:n.448-60_448-59del
ENST00000395951.7:c.679-60_679-59del	ENSP00000379281.3:n.679-60_679-59del
ENST00000395953.6:c.679-60_679-59del	ENSP00000379283.2:n.679-60_679-59del
ENST00000395956.7:c.679-60_679-59del	ENSP00000379286.3:n.679-60_679-59del
ENST00000395957.6:c.679-60_679-59del	ENSP00000379287.2:n.679-60_679-59del
ENST00000395958.5:c.679-60_679-59del	ENSP00000379288.2:n.679-60_679-59del
ENST00000419477.6:c.679-60_679-59del	ENSP00000395114.2:n.679-60_679-59del
ENST00000457309.2:c.679-60_679-59del	ENSP00000398599.1:n.679-60_679-59del
ENST00000521309.5:c.319-60_319-59del	ENSP00000429623.1:n.319-60_319-59del
ENST00000521607.5:c.703-60_703-59del	ENSP00000430058.1:n.703-60_703-59del
ENST00000522542.5:c.454-60_454-59del	ENSP00000430072.1:n.454-60_454-59del
ENST00000522819.5:c.319-60_319-59del	ENSP00000428775.1:n.319-60_319-59del
ENST00000523848.5:c.334-60_334-59del	ENSP00000428860.1:n.334-60_334-59del
NM_001135699.1:c.679-60_679-59del	NP_001129171.1:n.679-60_679-59del
NM_001135700.1:c.679-60_679-59del	NP_001129172.1:n.679-60_679-59del
NM_001135701.1:c.679-60_679-59del	NP_001129173.1:n.679-60_679-59del
NM_001135702.1:c.679-60_679-59del	NP_001129174.1:n.679-60_679-59del
NM_003406.3:c.679-60_679-59del	NP_003397.1:n.679-60_679-59del
NM_145690.2:c.679-60_679-59del	NP_663723.1:n.679-60_679-59del
XM_005251061.2:c.679-60_679-59del	XP_005251118.1:n.679-60_679-59del
XM_005251062.2:c.679-60_679-59del	XP_005251119.1:n.679-60_679-59del
XM_005251063.2:c.679-60_679-59del	XP_005251120.1:n.679-60_679-59del
XM_011517289.1:c.679-60_679-59del	XP_011515591.1:n.679-60_679-59del
XM_005251061.3:c.679-60_679-59del	XP_005251118.1:n.679-60_679-59del
XM_005251063.3:c.679-60_679-59del	XP_005251120.1:n.679-60_679-59del
XM_017013810.2:c.679-60_679-59del	XP_016869299.1:n.679-60_679-59del
XM_017013811.1:c.679-60_679-59del	XP_016869300.1:n.679-60_679-59del
XM_024447266.1:c.679-60_679-59del	XP_024303034.1:n.679-60_679-59del
NM_145690.3:c.679-60_679-59del MANE Select	NP_663723.1:n.679-60_679-59del
NM_001135700.2:c.679-60_679-59del	NP_001129172.1:n.679-60_679-59del
NM_001135701.2:c.679-60_679-59del	NP_001129173.1:n.679-60_679-59del
NM_001135702.2:c.679-60_679-59del	NP_001129174.1:n.679-60_679-59del
NM_003406.4:c.679-60_679-59del	NP_003397.1:n.679-60_679-59del
NM_001135699.2:c.679-60_679-59del	NP_001129171.1:n.679-60_679-59del