Canonical Allele Identifier: CA2576767512

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287827_38287836del , CM000681.2:g.38287827_38287836del	GRCh38
NC_000019.9:g.38778467_38778476del , CM000681.1:g.38778467_38778476del	GRCh37
NC_000019.8:g.43470307_43470316del	NCBI36
NG_013372.1:g.28370_28379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.278-49_278-40del MANE Select	ENSP00000301244.5:n.278-49_278-40del
ENST00000301244.11:c.278-49_278-40del	ENSP00000301244.5:n.278-49_278-40del
ENST00000454580.7:c.107-49_107-40del	ENSP00000389788.2:n.107-49_107-40del
ENST00000587090.5:c.128-49_128-40del	ENSP00000466407.1:n.128-49_128-40del
ENST00000587516.5:c.278-1311_278-1302del	ENSP00000465721.1:n.278-1311_278-1302del
ENST00000590210.1:n.475-49_475-40del
ENST00000590510.5:c.128-49_128-40del	ENSP00000465301.1:n.128-49_128-40del
ENST00000592007.1:c.128-49_128-40del	ENSP00000465561.1:n.128-49_128-40del
NM_001166103.1:c.107-49_107-40del	NP_001159575.1:n.107-49_107-40del
NM_021102.3:c.278-49_278-40del	NP_066925.1:n.278-49_278-40del
NM_021102.4:c.278-49_278-40del MANE Select	NP_066925.1:n.278-49_278-40del
NM_001166103.2:c.107-49_107-40del	NP_001159575.1:n.107-49_107-40del