Canonical Allele Identifier: CA14992576

Gene: YWHAH

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.31953076T>C , CM000684.2:g.31953076T>C	GRCh38
NC_000022.10:g.32349063T>C , CM000684.1:g.32349063T>C	GRCh37
NC_000022.9:g.30679063T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248975.6:c.88-3063T>C MANE Select	ENSP00000248975.5:n.88-3063T>C
ENST00000646701.1:c.1787-3063T>C	ENSP00000496158.1:n.1787-3063T>C
ENST00000248975.5:c.88-3063T>C	ENSP00000248975.5:n.88-3063T>C
ENST00000397492.1:c.202+2654T>C	ENSP00000380629.1:n.202+2654T>C
ENST00000420430.1:c.49-3063T>C	ENSP00000406747.1:n.49-3063T>C
ENST00000443669.5:c.*147-3063T>C	ENSP00000408468.1:n.*147-3063T>C
ENST00000471374.1:n.271-3063T>C
ENST00000479649.1:n.197-3063T>C
NM_003405.3:c.88-3063T>C	NP_003396.1:n.88-3063T>C
NM_003405.4:c.88-3063T>C MANE Select	NP_003396.1:n.88-3063T>C