Canonical Allele Identifier: CA2334951890

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287798_38287799delinsCA , CM000681.2:g.38287798_38287799delinsCA	GRCh38
NC_000019.9:g.38778438_38778439delinsCA , CM000681.1:g.38778438_38778439delinsCA	GRCh37
NC_000019.8:g.43470278_43470279delinsCA	NCBI36
NG_013372.1:g.28341_28342delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.278-78_278-77delinsCA MANE Select	ENSP00000301244.5:n.278-78_278-77delinsCA
ENST00000301244.11:c.278-78_278-77delinsCA	ENSP00000301244.5:n.278-78_278-77delinsCA
ENST00000454580.7:c.107-78_107-77delinsCA	ENSP00000389788.2:n.107-78_107-77delinsCA
ENST00000587090.5:c.128-78_128-77delinsCA	ENSP00000466407.1:n.128-78_128-77delinsCA
ENST00000587516.5:c.278-1340_278-1339delinsCA	ENSP00000465721.1:n.278-1340_278-1339delinsCA
ENST00000590210.1:n.475-78_475-77delinsCA
ENST00000590510.5:c.128-78_128-77delinsCA	ENSP00000465301.1:n.128-78_128-77delinsCA
ENST00000592007.1:c.128-78_128-77delinsCA	ENSP00000465561.1:n.128-78_128-77delinsCA
NM_001166103.1:c.107-78_107-77delinsCA	NP_001159575.1:n.107-78_107-77delinsCA
NM_021102.3:c.278-78_278-77delinsCA	NP_066925.1:n.278-78_278-77delinsCA
NM_021102.4:c.278-78_278-77delinsCA MANE Select	NP_066925.1:n.278-78_278-77delinsCA
NM_001166103.2:c.107-78_107-77delinsCA	NP_001159575.1:n.107-78_107-77delinsCA