Canonical Allele Identifier: CA213392

Gene: TEX15

Linked Data

• ClinVar Variation Id: 190036
• ClinVar RCV Id: RCV000202575 ; RCV000626476
• dbSNP Id: rs864309485
• MyVariant Identifiers: chr8:g.30704404A>C (hg19) ; chr8:g.30846888A>C (hg38)
• PubMed: PMID:26199321

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30846888A>C , CM000670.2:g.30846888A>C	GRCh38
NC_000008.10:g.30704404A>C , CM000670.1:g.30704404A>C	GRCh37
NC_000008.9:g.30823946A>C	NCBI36
NG_053141.1:g.71125T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256246.5:c.2130T>G	ENSP00000256246.2:p.Tyr710Ter
ENST00000638951.1:c.3291T>G	ENSP00000492713.1:p.Tyr1097Ter
ENST00000643185.2:c.3279T>G MANE Select	ENSP00000493555.1:p.Tyr1093Ter
ENST00000256246.4:c.2130T>G	ENSP00000256246.2:p.Tyr710Ter
NM_031271.3:c.2130T>G	NP_112561.2:p.Tyr710Ter
XM_005273575.2:c.3279T>G	XP_005273632.1:p.Tyr1093Ter
XM_005273576.2:c.2970T>G	XP_005273633.1:p.Tyr990Ter
XM_006716369.2:c.3279T>G	XP_006716432.1:p.Tyr1093Ter
XM_011544588.1:c.3291T>G	XP_011542890.1:p.Tyr1097Ter
XM_011544589.1:c.3279T>G	XP_011542891.1:p.Tyr1093Ter
XM_011544590.1:c.3279T>G	XP_011542892.1:p.Tyr1093Ter
XM_011544591.1:c.3279T>G	XP_011542893.1:p.Tyr1093Ter
XM_011544592.1:c.3279T>G	XP_011542894.1:p.Tyr1093Ter
XM_011544593.1:c.2970T>G	XP_011542895.1:p.Tyr990Ter
XM_011544594.1:c.3291T>G	XP_011542896.1:p.Tyr1097Ter
NM_001350162.1:c.3279T>G	NP_001337091.1:p.Tyr1093Ter
XM_006716369.4:c.3279T>G	XP_006716432.1:p.Tyr1093Ter
XM_011544588.2:c.3291T>G	XP_011542890.1:p.Tyr1097Ter
XM_011544589.3:c.3279T>G	XP_011542891.1:p.Tyr1093Ter
XM_011544590.3:c.3279T>G	XP_011542892.1:p.Tyr1093Ter
XM_011544591.3:c.3279T>G	XP_011542893.1:p.Tyr1093Ter
XM_011544592.3:c.3279T>G	XP_011542894.1:p.Tyr1093Ter
XM_011544593.3:c.2970T>G	XP_011542895.1:p.Tyr990Ter
XM_011544594.2:c.3291T>G	XP_011542896.1:p.Tyr1097Ter
XM_024447196.1:c.3279T>G	XP_024302964.1:p.Tyr1093Ter
XM_024447197.1:c.2970T>G	XP_024302965.1:p.Tyr990Ter
NM_001350162.2:c.3279T>G MANE Select	NP_001337091.1:p.Tyr1093Ter