Canonical Allele Identifier: CA2584810794

Gene: SPINT2

Linked Data

• gnomAD v4: 19-38287998-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287998C>A , CM000681.2:g.38287998C>A	GRCh38
NC_000019.9:g.38778638C>A , CM000681.1:g.38778638C>A	GRCh37
NC_000019.8:g.43470478C>A	NCBI36
NG_013372.1:g.28541C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+63C>A MANE Select	ENSP00000301244.5:n.337+63C>A
ENST00000301244.11:c.337+63C>A	ENSP00000301244.5:n.337+63C>A
ENST00000454580.7:c.166+63C>A	ENSP00000389788.2:n.166+63C>A
ENST00000587090.5:c.187+63C>A	ENSP00000466407.1:n.187+63C>A
ENST00000587516.5:c.278-1140C>A	ENSP00000465721.1:n.278-1140C>A
NM_001166103.1:c.166+63C>A	NP_001159575.1:n.166+63C>A
NM_021102.3:c.337+63C>A	NP_066925.1:n.337+63C>A
NM_021102.4:c.337+63C>A MANE Select	NP_066925.1:n.337+63C>A
NM_001166103.2:c.166+63C>A	NP_001159575.1:n.166+63C>A