Canonical Allele Identifier: CA1806088955

Gene: YWHAZ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100920574T= , CM000670.2:g.100920574T=	GRCh38
NC_000008.10:g.101932802T= , CM000670.1:g.101932802T=	GRCh37
NC_000008.9:g.102001978T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395958.6:c.*119A= MANE Select	ENSP00000379288.2:n.*119A=
ENST00000353245.7:c.*119A=	ENSP00000309503.3:n.*119A=
ENST00000395956.7:c.*119A=	ENSP00000379286.3:n.*119A=
ENST00000395957.6:c.*119A=	ENSP00000379287.2:n.*119A=
ENST00000395958.5:c.*119A=	ENSP00000379288.2:n.*119A=
ENST00000457309.2:c.*119A=	ENSP00000398599.1:n.*119A=
ENST00000521309.5:c.*119A=	ENSP00000429623.1:n.*119A=
ENST00000522542.5:c.*119A=	ENSP00000430072.1:n.*119A=
ENST00000522819.5:c.*119A=	ENSP00000428775.1:n.*119A=
ENST00000523848.5:c.496+16A=	ENSP00000428860.1:n.496+16A=
NM_001135699.1:c.*119A=	NP_001129171.1:n.*119A=
NM_001135700.1:c.*119A=	NP_001129172.1:n.*119A=
NM_001135701.1:c.*119A=	NP_001129173.1:n.*119A=
NM_001135702.1:c.*119A=	NP_001129174.1:n.*119A=
NM_003406.3:c.*119A=	NP_003397.1:n.*119A=
NM_145690.2:c.*119A=	NP_663723.1:n.*119A=
XM_005251061.2:c.*119A=	XP_005251118.1:n.*119A=
XM_005251062.2:c.*119A=	XP_005251119.1:n.*119A=
XM_005251063.2:c.*119A=	XP_005251120.1:n.*119A=
XM_011517289.1:c.*119A=	XP_011515591.1:n.*119A=
XM_005251061.3:c.*119A=	XP_005251118.1:n.*119A=
XM_005251063.3:c.*119A=	XP_005251120.1:n.*119A=
XM_017013810.2:c.*119A=	XP_016869299.1:n.*119A=
XM_017013811.1:c.*119A=	XP_016869300.1:n.*119A=
XM_024447266.1:c.*119A=	XP_024303034.1:n.*119A=
NM_145690.3:c.*119A= MANE Select	NP_663723.1:n.*119A=
NM_001135700.2:c.*119A=	NP_001129172.1:n.*119A=
NM_001135701.2:c.*119A=	NP_001129173.1:n.*119A=
NM_001135702.2:c.*119A=	NP_001129174.1:n.*119A=
NM_003406.4:c.*119A=	NP_003397.1:n.*119A=
NM_001135699.2:c.*119A=	NP_001129171.1:n.*119A=