Canonical Allele Identifier: CA13427365

Gene: YAP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102219736G>C , CM000673.2:g.102219736G>C	GRCh38
NC_000011.9:g.102090467G>C , CM000673.1:g.102090467G>C	GRCh37
NC_000011.8:g.101595677G>C	NCBI36
NG_029530.1:g.114276G>C
NG_029530.2:g.114276G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282441.10:c.1033-3886G>C MANE Select	ENSP00000282441.5:n.1033-3886G>C
ENST00000282441.9:c.1033-3886G>C	ENSP00000282441.5:n.1033-3886G>C
ENST00000345877.6:c.931-3886G>C	ENSP00000331023.4:n.931-3886G>C
ENST00000524575.5:c.499-3886G>C	ENSP00000435602.1:n.499-3886G>C
ENST00000526343.5:c.871-3886G>C	ENSP00000434134.1:n.871-3886G>C
ENST00000529029.1:c.294-3886G>C
ENST00000531439.5:c.985-3886G>C	ENSP00000431574.1:n.985-3886G>C
ENST00000537274.5:c.997-3886G>C	ENSP00000445635.1:n.997-3886G>C
ENST00000615667.4:c.1045-3886G>C	ENSP00000478927.1:n.1045-3886G>C
ENST00000629586.2:c.883-3886G>C	ENSP00000487519.1:n.883-3886G>C
NM_001130145.2:c.1033-3886G>C	NP_001123617.1:n.1033-3886G>C
NM_001195044.1:c.985-3886G>C	NP_001181973.1:n.985-3886G>C
NM_001195045.1:c.499-3886G>C	NP_001181974.1:n.499-3886G>C
NM_001282097.1:c.919-3886G>C	NP_001269026.1:n.919-3886G>C
NM_001282098.1:c.883-3886G>C	NP_001269027.1:n.883-3886G>C
NM_001282099.1:c.931-3886G>C	NP_001269028.1:n.931-3886G>C
NM_001282100.1:c.997-3886G>C	NP_001269029.1:n.997-3886G>C
NM_001282101.1:c.1045-3886G>C	NP_001269030.1:n.1045-3886G>C
NM_006106.4:c.871-3886G>C	NP_006097.2:n.871-3886G>C
XM_005271378.2:c.1051-3886G>C	XP_005271435.1:n.1051-3886G>C
XM_005271380.2:c.1039-3886G>C	XP_005271437.1:n.1039-3886G>C
XM_005271381.2:c.1003-3886G>C	XP_005271438.1:n.1003-3886G>C
XM_005271383.2:c.991-3886G>C	XP_005271440.1:n.991-3886G>C
XM_011542555.1:c.517-3886G>C	XP_011540857.1:n.517-3886G>C
XM_011542556.1:c.511-3886G>C	XP_011540858.1:n.511-3886G>C
XM_005271378.3:c.1051-3886G>C	XP_005271435.1:n.1051-3886G>C
XM_005271380.3:c.1039-3886G>C	XP_005271437.1:n.1039-3886G>C
XM_005271381.3:c.1003-3886G>C	XP_005271438.1:n.1003-3886G>C
XM_005271383.3:c.991-3886G>C	XP_005271440.1:n.991-3886G>C
XM_011542555.2:c.517-3886G>C	XP_011540857.1:n.517-3886G>C
XM_011542556.2:c.511-3886G>C	XP_011540858.1:n.511-3886G>C
XM_017017093.1:c.451-3886G>C	XP_016872582.1:n.451-3886G>C
NM_001130145.3:c.1033-3886G>C MANE Select	NP_001123617.1:n.1033-3886G>C
NM_001195044.2:c.985-3886G>C	NP_001181973.1:n.985-3886G>C
NM_001195045.2:c.499-3886G>C	NP_001181974.1:n.499-3886G>C
NM_001282097.2:c.919-3886G>C	NP_001269026.1:n.919-3886G>C
NM_001282098.2:c.883-3886G>C	NP_001269027.1:n.883-3886G>C
NM_006106.5:c.871-3886G>C	NP_006097.2:n.871-3886G>C
NM_001282099.2:c.931-3886G>C	NP_001269028.1:n.931-3886G>C
NM_001282100.2:c.997-3886G>C	NP_001269029.1:n.997-3886G>C
NM_001282101.2:c.1045-3886G>C	NP_001269030.1:n.1045-3886G>C