Canonical Allele Identifier: CA2334951941

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287928C= , CM000681.2:g.38287928C=	GRCh38
NC_000019.9:g.38778568C= , CM000681.1:g.38778568C=	GRCh37
NC_000019.8:g.43470408C=	NCBI36
NG_013372.1:g.28471C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.330C= MANE Select	ENSP00000301244.5:p.Val110=
ENST00000301244.11:c.330C=	ENSP00000301244.5:p.Val110=
ENST00000454580.7:c.159C=	ENSP00000389788.2:p.Val53=
ENST00000587090.5:c.180C=	ENSP00000466407.1:p.Val60=
ENST00000587516.5:c.278-1210C=	ENSP00000465721.1:n.278-1210C=
ENST00000590210.1:n.527C=
ENST00000592007.1:c.180C=	ENSP00000465561.1:p.Val60=
NM_001166103.1:c.159C=	NP_001159575.1:p.Val53=
NM_021102.3:c.330C=	NP_066925.1:p.Val110=
NM_021102.4:c.330C= MANE Select	NP_066925.1:p.Val110=
NM_001166103.2:c.159C=	NP_001159575.1:p.Val53=