Canonical Allele Identifier: CA2584810803

Gene: SPINT2

Linked Data

• gnomAD v4: 19-38288027-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38288027_38288028insAA , CM000681.2:g.38288027_38288028insAA	GRCh38
NC_000019.9:g.38778667_38778668insAA , CM000681.1:g.38778667_38778668insAA	GRCh37
NC_000019.8:g.43470507_43470508insAA	NCBI36
NG_013372.1:g.28570_28571insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+92_337+93insAA MANE Select	ENSP00000301244.5:n.337+92_337+93insAA
ENST00000301244.11:c.337+92_337+93insAA	ENSP00000301244.5:n.337+92_337+93insAA
ENST00000454580.7:c.166+92_166+93insAA	ENSP00000389788.2:n.166+92_166+93insAA
ENST00000587090.5:c.187+92_187+93insAA	ENSP00000466407.1:n.187+92_187+93insAA
ENST00000587516.5:c.278-1111_278-1110insAA	ENSP00000465721.1:n.278-1111_278-1110insAA
NM_001166103.1:c.166+92_166+93insAA	NP_001159575.1:n.166+92_166+93insAA
NM_021102.3:c.337+92_337+93insAA	NP_066925.1:n.337+92_337+93insAA
NM_021102.4:c.337+92_337+93insAA MANE Select	NP_066925.1:n.337+92_337+93insAA
NM_001166103.2:c.166+92_166+93insAA	NP_001159575.1:n.166+92_166+93insAA