Canonical Allele Identifier: CA2334952047

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38288160_38288161delinsTC , CM000681.2:g.38288160_38288161delinsTC	GRCh38
NC_000019.9:g.38778800_38778801delinsTC , CM000681.1:g.38778800_38778801delinsTC	GRCh37
NC_000019.8:g.43470640_43470641delinsTC	NCBI36
NG_013372.1:g.28703_28704delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+225_337+226delinsTC MANE Select	ENSP00000301244.5:n.337+225_337+226delinsTC
ENST00000301244.11:c.337+225_337+226delinsTC	ENSP00000301244.5:n.337+225_337+226delinsTC
ENST00000454580.7:c.166+225_166+226delinsTC	ENSP00000389788.2:n.166+225_166+226delinsTC
ENST00000587090.5:c.187+225_187+226delinsTC	ENSP00000466407.1:n.187+225_187+226delinsTC
ENST00000587516.5:c.278-978_278-977delinsTC	ENSP00000465721.1:n.278-978_278-977delinsTC
NM_001166103.1:c.166+225_166+226delinsTC	NP_001159575.1:n.166+225_166+226delinsTC
NM_021102.3:c.337+225_337+226delinsTC	NP_066925.1:n.337+225_337+226delinsTC
NM_021102.4:c.337+225_337+226delinsTC MANE Select	NP_066925.1:n.337+225_337+226delinsTC
NM_001166103.2:c.166+225_166+226delinsTC	NP_001159575.1:n.166+225_166+226delinsTC