Canonical Allele Identifier: CA657714636

Gene: TEX11

Linked Data

• COSMIC: COSN9095469 ; COSN15525050

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853205T>G , CM000685.2:g.70853205T>G	GRCh38
NC_000023.10:g.70073055T>G , CM000685.1:g.70073055T>G	GRCh37
NC_000023.9:g.69989780T>G	NCBI36
NG_012574.1:g.60513A>C
NG_012574.2:g.60513A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.405+43A>C MANE Select	ENSP00000363453.2:n.405+43A>C
ENST00000344304.3:c.450+43A>C	ENSP00000340995.3:n.450+43A>C
ENST00000374333.6:c.405+43A>C	ENSP00000363453.2:n.405+43A>C
ENST00000395889.6:c.450+43A>C	ENSP00000379226.2:n.450+43A>C
NM_001003811.1:c.450+43A>C	NP_001003811.1:n.450+43A>C
NM_031276.2:c.405+43A>C	NP_112566.2:n.405+43A>C
XM_011530994.1:c.405+43A>C	XP_011529296.1:n.405+43A>C
XM_017029649.1:c.405+43A>C	XP_016885138.1:n.405+43A>C
NM_001003811.2:c.450+43A>C	NP_001003811.1:n.450+43A>C
NM_031276.3:c.405+43A>C MANE Select	NP_112566.2:n.405+43A>C