Canonical Allele Identifier: CA2581058630

Gene: YAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102199908A>C , CM000673.2:g.102199908A>C	GRCh38
NC_000011.9:g.102070639A>C , CM000673.1:g.102070639A>C	GRCh37
NC_000011.8:g.101575849A>C	NCBI36
NG_029530.1:g.94448A>C
NG_029530.2:g.94448A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001130145.3:c.803-5985A>C MANE Select	NP_001123617.1:n.803-5985A>C
ENST00000282441.10:c.803-5985A>C MANE Select	ENSP00000282441.5:n.803-5985A>C
NM_001130145.2:c.803-5985A>C	NP_001123617.1:n.803-5985A>C
NM_001195044.1:c.803-5985A>C	NP_001181973.1:n.803-5985A>C
NM_001195044.2:c.803-5985A>C	NP_001181973.1:n.803-5985A>C
NM_001195045.1:c.269-5985A>C	NP_001181974.1:n.269-5985A>C
NM_001195045.2:c.269-5985A>C	NP_001181974.1:n.269-5985A>C
NM_001282097.1:c.689-5985A>C	NP_001269026.1:n.689-5985A>C
NM_001282097.2:c.689-5985A>C	NP_001269026.1:n.689-5985A>C
NM_001282098.1:c.689-5985A>C	NP_001269027.1:n.689-5985A>C
NM_001282098.2:c.689-5985A>C	NP_001269027.1:n.689-5985A>C
NM_001282099.1:c.689-5985A>C	NP_001269028.1:n.689-5985A>C
NM_001282099.2:c.689-5985A>C	NP_001269028.1:n.689-5985A>C
NM_001282100.1:c.803-5985A>C	NP_001269029.1:n.803-5985A>C
NM_001282100.2:c.803-5985A>C	NP_001269029.1:n.803-5985A>C
NM_001282101.1:c.803-5985A>C	NP_001269030.1:n.803-5985A>C
NM_001282101.2:c.803-5985A>C	NP_001269030.1:n.803-5985A>C
NM_006106.4:c.689-5985A>C	NP_006097.2:n.689-5985A>C
NM_006106.5:c.689-5985A>C	NP_006097.2:n.689-5985A>C
ENST00000282441.9:c.803-5985A>C	ENSP00000282441.5:n.803-5985A>C
ENST00000345877.6:c.689-5985A>C	ENSP00000331023.4:n.689-5985A>C
ENST00000524575.5:c.269-5985A>C	ENSP00000435602.1:n.269-5985A>C
ENST00000526343.5:c.689-5985A>C	ENSP00000434134.1:n.689-5985A>C
ENST00000529029.1:c.52-5985A>C
ENST00000531439.5:c.803-5985A>C	ENSP00000431574.1:n.803-5985A>C
ENST00000537274.5:c.803-5985A>C	ENSP00000445635.1:n.803-5985A>C
ENST00000615667.4:c.803-5985A>C	ENSP00000478927.1:n.803-5985A>C
ENST00000629586.2:c.689-5985A>C	ENSP00000487519.1:n.689-5985A>C
XM_005271378.2:c.809-5985A>C	XP_005271435.1:n.809-5985A>C
XM_005271378.3:c.809-5985A>C	XP_005271435.1:n.809-5985A>C
XM_005271380.2:c.809-5985A>C	XP_005271437.1:n.809-5985A>C
XM_005271380.3:c.809-5985A>C	XP_005271437.1:n.809-5985A>C
XM_005271381.2:c.809-5985A>C	XP_005271438.1:n.809-5985A>C
XM_005271381.3:c.809-5985A>C	XP_005271438.1:n.809-5985A>C
XM_005271383.2:c.809-5985A>C	XP_005271440.1:n.809-5985A>C
XM_005271383.3:c.809-5985A>C	XP_005271440.1:n.809-5985A>C
XM_011542555.1:c.275-5985A>C	XP_011540857.1:n.275-5985A>C
XM_011542555.2:c.275-5985A>C	XP_011540857.1:n.275-5985A>C
XM_011542556.1:c.269-5985A>C	XP_011540858.1:n.269-5985A>C
XM_011542556.2:c.269-5985A>C	XP_011540858.1:n.269-5985A>C
XM_017017093.1:c.269-5985A>C	XP_016872582.1:n.269-5985A>C