Canonical Allele Identifier: CA4749994

Gene: TCEA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.53970412C>G , CM000670.2:g.53970412C>G	GRCh38
NC_000008.10:g.54882972C>G , CM000670.1:g.54882972C>G	GRCh37
NC_000008.9:g.55045525C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006756.4:c.877G>C MANE Select	NP_006747.1:p.Glu293Gln
ENST00000521604.7:c.877G>C MANE Select	ENSP00000428426.2:p.Glu293Gln
NM_006756.3:c.877G>C	NP_006747.1:p.Glu293Gln
NM_201437.2:c.814G>C	NP_958845.1:p.Glu272Gln
NM_201437.3:c.814G>C	NP_958845.1:p.Glu272Gln
NR_109901.1:n.1584G>C
NR_109901.2:n.1576G>C
NR_109902.1:n.656G>C
NR_109902.2:n.648G>C
ENST00000396401.7:c.814G>C	ENSP00000395483.2:p.Glu272Gln
ENST00000521086.6:n.1393G>C
ENST00000521604.6:c.877G>C	ENSP00000428426.2:p.Glu293Gln
ENST00000522397.5:n.704G>C
ENST00000522635.5:c.325G>C	ENSP00000429192.1:p.Glu109Gln
ENST00000640041.1:c.814G>C	ENSP00000492389.1:p.Glu272Gln
ENST00000640382.1:c.877G>C	ENSP00000491445.1:p.Glu293Gln
XM_006716467.1:c.736G>C	XP_006716530.1:p.Glu246Gln
XM_011517578.1:c.772G>C	XP_011515880.1:p.Glu258Gln
XM_011517579.1:c.736G>C	XP_011515881.1:p.Glu246Gln