Canonical Allele Identifier: CA13270243

Gene: TSPAN14

Linked Data

• dbSNP Id: rs6586030
• gnomAD v2: 10-82254047-A-G
• gnomAD v3: 10-80494291-A-G
• gnomAD v4: 10-80494291-A-G
• MyVariant Identifiers: chr10:g.82254047A>G (hg19) ; chr10:g.80494291A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80494291A>G , CM000672.2:g.80494291A>G	GRCh38
NC_000010.10:g.82254047A>G , CM000672.1:g.82254047A>G	GRCh37
NC_000010.9:g.82244027A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429989.8:c.81+4977A>G MANE Select	ENSP00000396270.2:n.81+4977A>G
ENST00000372158.6:c.81+4977A>G	ENSP00000361231.1:n.81+4977A>G
ENST00000341863.10:c.81+4977A>G	ENSP00000344076.6:n.81+4977A>G
ENST00000372156.5:c.81+4977A>G	ENSP00000361229.1:n.81+4977A>G
ENST00000372157.6:c.-39+4977A>G	ENSP00000361230.2:n.-39+4977A>G
ENST00000372158.5:c.81+4977A>G	ENSP00000361231.1:n.81+4977A>G
ENST00000372164.7:c.81+4977A>G	ENSP00000361237.3:n.81+4977A>G
ENST00000429989.7:c.81+4977A>G	ENSP00000396270.2:n.81+4977A>G
ENST00000469149.1:n.141+4977A>G
ENST00000481124.5:c.81+4977A>G	ENSP00000418195.1:n.81+4977A>G
ENST00000616406.1:c.81+4977A>G	ENSP00000480263.1:n.81+4977A>G
NM_001128309.1:c.81+4977A>G	NP_001121781.1:n.81+4977A>G
NM_030927.2:c.81+4977A>G	NP_112189.2:n.81+4977A>G
XM_006717992.2:c.81+4977A>G	XP_006718055.1:n.81+4977A>G
XM_011540218.1:c.126+3206A>G	XP_011538520.1:n.126+3206A>G
XM_011540219.1:c.81+4977A>G	XP_011538521.1:n.81+4977A>G
XM_011540220.1:c.81+4977A>G	XP_011538522.1:n.81+4977A>G
XM_011540221.1:c.81+4977A>G	XP_011538523.1:n.81+4977A>G
XM_011540222.1:c.81+4977A>G	XP_011538524.1:n.81+4977A>G
NM_001128309.2:c.81+4977A>G	NP_001121781.1:n.81+4977A>G
NM_001351266.1:c.81+4977A>G	NP_001338195.1:n.81+4977A>G
NM_001351267.1:c.81+4977A>G	NP_001338196.1:n.81+4977A>G
NM_001351268.1:c.81+4977A>G	NP_001338197.1:n.81+4977A>G
NM_001351269.1:c.81+4977A>G	NP_001338198.1:n.81+4977A>G
NM_001351270.1:c.81+4977A>G	NP_001338199.1:n.81+4977A>G
NM_001351271.1:c.81+4977A>G	NP_001338200.1:n.81+4977A>G
NM_001351272.1:c.81+4977A>G	NP_001338201.1:n.81+4977A>G
NM_030927.3:c.81+4977A>G	NP_112189.2:n.81+4977A>G
XM_011540219.3:c.81+4977A>G	XP_011538521.1:n.81+4977A>G
XM_011540220.3:c.81+4977A>G	XP_011538522.1:n.81+4977A>G
XM_011540221.3:c.81+4977A>G	XP_011538523.1:n.81+4977A>G
XM_017016712.2:c.-39+4977A>G	XP_016872201.1:n.-39+4977A>G
XM_017016713.2:c.-39+4977A>G	XP_016872202.1:n.-39+4977A>G
XM_024448211.1:c.81+4977A>G	XP_024303979.1:n.81+4977A>G
XM_024448212.1:c.81+4977A>G	XP_024303980.1:n.81+4977A>G
NM_001351267.3:c.81+4977A>G	NP_001338196.1:n.81+4977A>G
NM_001128309.3:c.81+4977A>G	NP_001121781.1:n.81+4977A>G
NM_001351266.2:c.81+4977A>G	NP_001338195.1:n.81+4977A>G
NM_001351267.4:c.81+4977A>G	NP_001338196.1:n.81+4977A>G
NM_001351268.2:c.81+4977A>G	NP_001338197.1:n.81+4977A>G
NM_001351269.2:c.81+4977A>G	NP_001338198.1:n.81+4977A>G
NM_001351270.2:c.81+4977A>G	NP_001338199.1:n.81+4977A>G
NM_001351271.2:c.81+4977A>G	NP_001338200.1:n.81+4977A>G
NM_001351272.2:c.81+4977A>G	NP_001338201.1:n.81+4977A>G
NM_030927.4:c.81+4977A>G MANE Select	NP_112189.2:n.81+4977A>G