Canonical Allele Identifier: CA593845032

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1481070050
• gnomAD v2: 10-71245563-G-C
• gnomAD v3: 10-69485807-G-C
• gnomAD v4: 10-69485807-G-C
• MyVariant Identifiers: chr10:g.71245563G>C (hg19) ; chr10:g.69485807G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485807G>C , CM000672.2:g.69485807G>C	GRCh38
NC_000010.10:g.71245563G>C , CM000672.1:g.71245563G>C	GRCh37
NC_000010.9:g.70915569G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+592G>C MANE Select	ENSP00000362387.2:n.357+592G>C
ENST00000373290.6:c.357+592G>C	ENSP00000362387.2:n.357+592G>C
ENST00000452130.1:c.84+592G>C	ENSP00000404528.1:n.84+592G>C
ENST00000475069.5:n.127+592G>C
NM_012339.3:c.357+592G>C	NP_036471.1:n.357+592G>C
XM_005269667.3:c.97-9787G>C	XP_005269724.1:n.97-9787G>C
XM_006717738.2:c.285+592G>C	XP_006717801.1:n.285+592G>C
XR_945642.1:n.487+592G>C
NM_001351263.1:c.97-9787G>C	NP_001338192.1:n.97-9787G>C
NM_012339.4:c.357+592G>C	NP_036471.1:n.357+592G>C
NR_147091.1:n.485+592G>C
XM_017016010.1:c.357+592G>C	XP_016871499.1:n.357+592G>C
XR_001747072.1:n.488+592G>C
XR_001747073.1:n.488+592G>C
XR_001747074.1:n.485+592G>C
NM_012339.5:c.357+592G>C MANE Select	NP_036471.1:n.357+592G>C
NM_001351263.2:c.97-9787G>C	NP_001338192.1:n.97-9787G>C
NR_147091.2:n.487+592G>C