Canonical Allele Identifier: CA980668004

Gene: YWHAE

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1391601A>G , CM000679.2:g.1391601A>G	GRCh38
NC_000017.10:g.1294895A>G , CM000679.1:g.1294895A>G	GRCh37
NC_000017.9:g.1241645A>G	NCBI36
NG_009233.1:g.13662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264335.13:c.64+8446T>C MANE Select	ENSP00000264335.8:n.64+8446T>C
ENST00000264335.12:c.64+8446T>C	ENSP00000264335.8:n.64+8446T>C
ENST00000469398.5:n.105+8446T>C
ENST00000486241.1:n.163+8446T>C
ENST00000489287.1:n.154+8446T>C
ENST00000571732.5:c.-36+8446T>C	ENSP00000461762.1:n.-36+8446T>C
ENST00000573026.1:c.64+8446T>C	ENSP00000458386.1:n.64+8446T>C
ENST00000573196.5:c.64+8446T>C	ENSP00000461766.1:n.64+8446T>C
ENST00000575977.1:c.64+8446T>C	ENSP00000460712.1:n.64+8446T>C
NM_006761.4:c.64+8446T>C	NP_006752.1:n.64+8446T>C
NR_024058.1:n.216+8446T>C
XM_005256784.2:c.64+8446T>C	XP_005256841.1:n.64+8446T>C
XM_005256784.4:c.64+8446T>C	XP_005256841.1:n.64+8446T>C
XM_017025005.2:c.-36+8446T>C	XP_016880494.1:n.-36+8446T>C
NM_006761.5:c.64+8446T>C MANE Select	NP_006752.1:n.64+8446T>C
NR_024058.2:n.176+8446T>C