Canonical Allele Identifier: CA2334952002

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38288067G= , CM000681.2:g.38288067G=	GRCh38
NC_000019.9:g.38778707G= , CM000681.1:g.38778707G=	GRCh37
NC_000019.8:g.43470547G=	NCBI36
NG_013372.1:g.28610G=

Transcript Alleles

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