Canonical Allele Identifier: CA6593065

Gene: TNS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53063436C>G , CM000674.2:g.53063436C>G	GRCh38
NC_000012.11:g.53457220C>G , CM000674.1:g.53457220C>G	GRCh37
NC_000012.10:g.51743487C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_170754.4:c.4061+19C>G MANE Select	NP_736610.2:n.4061+19C>G
ENST00000314250.11:c.4061+19C>G MANE Select	ENSP00000319684.7:n.4061+19C>G
NM_015319.2:c.4091+19C>G	NP_056134.2:n.4091+19C>G
NM_170754.2:c.4061+19C>G	NP_736610.2:n.4061+19C>G
NM_198316.1:c.3689+19C>G	NP_938072.1:n.3689+19C>G
NM_198316.2:c.3689+19C>G	NP_938072.1:n.3689+19C>G
ENST00000314250.10:c.4061+19C>G	ENSP00000319684.6:n.4061+19C>G
ENST00000314276.7:c.4091+19C>G	ENSP00000319756.3:n.4091+19C>G
ENST00000379902.7:c.3689+19C>G	ENSP00000369232.3:n.3689+19C>G
ENST00000546602.5:c.3770+19C>G	ENSP00000449363.1:n.3770+19C>G
ENST00000549311.7:n.4345+19C>G
ENST00000549700.5:c.3866+19C>G	ENSP00000449361.1:n.3866+19C>G
ENST00000550048.1:n.446C>G
ENST00000552168.1:n.1319+19C>G
ENST00000552570.5:c.4055+19C>G	ENSP00000447021.1:n.4055+19C>G
XM_006719302.2:c.4118+19C>G	XP_006719365.1:n.4118+19C>G
XM_006719302.3:c.4118+19C>G	XP_006719365.1:n.4118+19C>G
XM_006719303.1:c.4088+19C>G	XP_006719366.1:n.4088+19C>G
XM_011538079.1:c.4043+19C>G	XP_011536381.1:n.4043+19C>G
XM_017019088.1:c.4088+19C>G	XP_016874577.1:n.4088+19C>G
XM_017019089.1:c.4070+19C>G	XP_016874578.1:n.4070+19C>G
XR_001748642.1:n.5385+19C>G