Canonical Allele Identifier: CA2334952001

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38288067_38288070delinsGCTC , CM000681.2:g.38288067_38288070delinsGCTC	GRCh38
NC_000019.9:g.38778707_38778710delinsGCTC , CM000681.1:g.38778707_38778710delinsGCTC	GRCh37
NC_000019.8:g.43470547_43470550delinsGCTC	NCBI36
NG_013372.1:g.28610_28613delinsGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+132_337+135delinsGCTC MANE Select	ENSP00000301244.5:n.337+132_337+135delinsGCTC
ENST00000301244.11:c.337+132_337+135delinsGCTC	ENSP00000301244.5:n.337+132_337+135delinsGCTC
ENST00000454580.7:c.166+132_166+135delinsGCTC	ENSP00000389788.2:n.166+132_166+135delinsGCTC
ENST00000587090.5:c.187+132_187+135delinsGCTC	ENSP00000466407.1:n.187+132_187+135delinsGCTC
ENST00000587516.5:c.278-1071_278-1068delinsGCTC	ENSP00000465721.1:n.278-1071_278-1068delinsGCTC
NM_001166103.1:c.166+132_166+135delinsGCTC	NP_001159575.1:n.166+132_166+135delinsGCTC
NM_021102.3:c.337+132_337+135delinsGCTC	NP_066925.1:n.337+132_337+135delinsGCTC
NM_021102.4:c.337+132_337+135delinsGCTC MANE Select	NP_066925.1:n.337+132_337+135delinsGCTC
NM_001166103.2:c.166+132_166+135delinsGCTC	NP_001159575.1:n.166+132_166+135delinsGCTC