Canonical Allele Identifier: CA584007064

Gene: YWHAZ

Linked Data

• dbSNP Id: rs1406964795
• gnomAD v2: 8-101932804-GAAGT-G
• gnomAD v3: 8-100920576-GAAGT-G
• gnomAD v4: 8-100920576-GAAGT-G
• MyVariant Identifiers: chr8:g.101932805_101932808del (hg19) ; chr8:g.100920577_100920580del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100920579_100920582del , CM000670.2:g.100920579_100920582del	GRCh38
NC_000008.10:g.101932807_101932810del , CM000670.1:g.101932807_101932810del	GRCh37
NC_000008.9:g.102001983_102001986del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395958.6:c.*113_*116del MANE Select	ENSP00000379288.2:n.*113_*116del
ENST00000353245.7:c.*113_*116del	ENSP00000309503.3:n.*113_*116del
ENST00000395956.7:c.*113_*116del	ENSP00000379286.3:n.*113_*116del
ENST00000395957.6:c.*113_*116del	ENSP00000379287.2:n.*113_*116del
ENST00000395958.5:c.*113_*116del	ENSP00000379288.2:n.*113_*116del
ENST00000457309.2:c.*113_*116del	ENSP00000398599.1:n.*113_*116del
ENST00000521309.5:c.*113_*116del	ENSP00000429623.1:n.*113_*116del
ENST00000522542.5:c.*113_*116del	ENSP00000430072.1:n.*113_*116del
ENST00000522819.5:c.*113_*116del	ENSP00000428775.1:n.*113_*116del
ENST00000523848.5:c.496+10_496+13del	ENSP00000428860.1:n.496+10_496+13del
NM_001135699.1:c.*113_*116del	NP_001129171.1:n.*113_*116del
NM_001135700.1:c.*113_*116del	NP_001129172.1:n.*113_*116del
NM_001135701.1:c.*113_*116del	NP_001129173.1:n.*113_*116del
NM_001135702.1:c.*113_*116del	NP_001129174.1:n.*113_*116del
NM_003406.3:c.*113_*116del	NP_003397.1:n.*113_*116del
NM_145690.2:c.*113_*116del	NP_663723.1:n.*113_*116del
XM_005251061.2:c.*113_*116del	XP_005251118.1:n.*113_*116del
XM_005251062.2:c.*113_*116del	XP_005251119.1:n.*113_*116del
XM_005251063.2:c.*113_*116del	XP_005251120.1:n.*113_*116del
XM_011517289.1:c.*113_*116del	XP_011515591.1:n.*113_*116del
XM_005251061.3:c.*113_*116del	XP_005251118.1:n.*113_*116del
XM_005251063.3:c.*113_*116del	XP_005251120.1:n.*113_*116del
XM_017013810.2:c.*113_*116del	XP_016869299.1:n.*113_*116del
XM_017013811.1:c.*113_*116del	XP_016869300.1:n.*113_*116del
XM_024447266.1:c.*113_*116del	XP_024303034.1:n.*113_*116del
NM_145690.3:c.*113_*116del MANE Select	NP_663723.1:n.*113_*116del
NM_001135700.2:c.*113_*116del	NP_001129172.1:n.*113_*116del
NM_001135701.2:c.*113_*116del	NP_001129173.1:n.*113_*116del
NM_001135702.2:c.*113_*116del	NP_001129174.1:n.*113_*116del
NM_003406.4:c.*113_*116del	NP_003397.1:n.*113_*116del
NM_001135699.2:c.*113_*116del	NP_001129171.1:n.*113_*116del