Canonical Allele Identifier: CA882041372

Gene: SPINT2

Linked Data

• dbSNP Id: rs1482058850
• gnomAD v3: 19-38287689-T-TA
• gnomAD v4: 19-38287689-T-TA
• MyVariant Identifiers: chr19:g.38778329_38778330insA (hg19) ; chr19:g.38287689_38287690insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287691dup , CM000681.2:g.38287691dup	GRCh38
NC_000019.9:g.38778331dup , CM000681.1:g.38778331dup	GRCh37
NC_000019.8:g.43470171dup	NCBI36
NG_013372.1:g.28234dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.278-185dup MANE Select	ENSP00000301244.5:n.278-185dup
ENST00000301244.11:c.278-185dup	ENSP00000301244.5:n.278-185dup
ENST00000454580.7:c.107-185dup	ENSP00000389788.2:n.107-185dup
ENST00000587090.5:c.128-185dup	ENSP00000466407.1:n.128-185dup
ENST00000587516.5:c.278-1447dup	ENSP00000465721.1:n.278-1447dup
ENST00000590210.1:n.475-185dup
ENST00000590510.5:c.128-185dup	ENSP00000465301.1:n.128-185dup
ENST00000592007.1:c.128-185dup	ENSP00000465561.1:n.128-185dup
NM_001166103.1:c.107-185dup	NP_001159575.1:n.107-185dup
NM_021102.3:c.278-185dup	NP_066925.1:n.278-185dup
NM_021102.4:c.278-185dup MANE Select	NP_066925.1:n.278-185dup
NM_001166103.2:c.107-185dup	NP_001159575.1:n.107-185dup