Canonical Allele Identifier: CA209271609

Gene: TSPAN15

Linked Data

• dbSNP Id: rs567460372
• gnomAD v2: 10-71263226-T-C
• gnomAD v3: 10-69503470-T-C
• gnomAD v4: 10-69503470-T-C
• MyVariant Identifiers: chr10:g.71263226T>C (hg19) ; chr10:g.69503470T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503470T>C , CM000672.2:g.69503470T>C	GRCh38
NC_000010.10:g.71263226T>C , CM000672.1:g.71263226T>C	GRCh37
NC_000010.9:g.70933232T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.571-968T>C MANE Select	ENSP00000362387.2:n.571-968T>C
ENST00000373290.6:c.571-968T>C	ENSP00000362387.2:n.571-968T>C
ENST00000452130.1:c.298-968T>C	ENSP00000404528.1:n.298-968T>C
ENST00000459981.1:n.503-968T>C
ENST00000475069.5:n.341-968T>C
ENST00000486093.5:n.280-968T>C
ENST00000490083.5:n.517-968T>C
NM_012339.3:c.571-968T>C	NP_036471.1:n.571-968T>C
XM_005269666.3:c.376-968T>C	XP_005269723.1:n.376-968T>C
XM_005269667.3:c.310-968T>C	XP_005269724.1:n.310-968T>C
XM_006717738.2:c.499-968T>C	XP_006717801.1:n.499-968T>C
XM_011539562.1:c.223-968T>C	XP_011537864.1:n.223-968T>C
XM_011539563.1:c.139-968T>C	XP_011537865.1:n.139-968T>C
XR_945642.1:n.772-968T>C
NM_001351263.1:c.310-968T>C	NP_001338192.1:n.310-968T>C
NM_012339.4:c.571-968T>C	NP_036471.1:n.571-968T>C
NR_147091.1:n.770-968T>C
XM_005269666.4:c.376-968T>C	XP_005269723.1:n.376-968T>C
XM_011539562.2:c.223-968T>C	XP_011537864.1:n.223-968T>C
XM_011539563.2:c.139-968T>C	XP_011537865.1:n.139-968T>C
XM_017016010.1:c.642-968T>C	XP_016871499.1:n.642-968T>C
XR_001747072.1:n.773-968T>C
XR_001747073.1:n.773-968T>C
XR_001747074.1:n.699-968T>C
NM_012339.5:c.571-968T>C MANE Select	NP_036471.1:n.571-968T>C
NM_001351263.2:c.310-968T>C	NP_001338192.1:n.310-968T>C
NR_147091.2:n.772-968T>C