Canonical Allele Identifier: CA2334951958

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287960_38287961delinsTG , CM000681.2:g.38287960_38287961delinsTG	GRCh38
NC_000019.9:g.38778600_38778601delinsTG , CM000681.1:g.38778600_38778601delinsTG	GRCh37
NC_000019.8:g.43470440_43470441delinsTG	NCBI36
NG_013372.1:g.28503_28504delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+25_337+26delinsTG MANE Select	ENSP00000301244.5:n.337+25_337+26delinsTG
ENST00000301244.11:c.337+25_337+26delinsTG	ENSP00000301244.5:n.337+25_337+26delinsTG
ENST00000454580.7:c.166+25_166+26delinsTG	ENSP00000389788.2:n.166+25_166+26delinsTG
ENST00000587090.5:c.187+25_187+26delinsTG	ENSP00000466407.1:n.187+25_187+26delinsTG
ENST00000587516.5:c.278-1178_278-1177delinsTG	ENSP00000465721.1:n.278-1178_278-1177delinsTG
ENST00000590210.1:n.559_560delinsTG
NM_001166103.1:c.166+25_166+26delinsTG	NP_001159575.1:n.166+25_166+26delinsTG
NM_021102.3:c.337+25_337+26delinsTG	NP_066925.1:n.337+25_337+26delinsTG
NM_021102.4:c.337+25_337+26delinsTG MANE Select	NP_066925.1:n.337+25_337+26delinsTG
NM_001166103.2:c.166+25_166+26delinsTG	NP_001159575.1:n.166+25_166+26delinsTG