Canonical Allele Identifier: CA2334952054

Gene: SPINT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38288176_38288179delinsTCTC , CM000681.2:g.38288176_38288179delinsTCTC	GRCh38
NC_000019.9:g.38778816_38778819delinsTCTC , CM000681.1:g.38778816_38778819delinsTCTC	GRCh37
NC_000019.8:g.43470656_43470659delinsTCTC	NCBI36
NG_013372.1:g.28719_28722delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+241_337+244delinsTCTC MANE Select	ENSP00000301244.5:n.337+241_337+244delinsTCTC
ENST00000301244.11:c.337+241_337+244delinsTCTC	ENSP00000301244.5:n.337+241_337+244delinsTCTC
ENST00000454580.7:c.166+241_166+244delinsTCTC	ENSP00000389788.2:n.166+241_166+244delinsTCTC
ENST00000587090.5:c.187+241_187+244delinsTCTC	ENSP00000466407.1:n.187+241_187+244delinsTCTC
ENST00000587516.5:c.278-962_278-959delinsTCTC	ENSP00000465721.1:n.278-962_278-959delinsTCTC
NM_001166103.1:c.166+241_166+244delinsTCTC	NP_001159575.1:n.166+241_166+244delinsTCTC
NM_021102.3:c.337+241_337+244delinsTCTC	NP_066925.1:n.337+241_337+244delinsTCTC
NM_021102.4:c.337+241_337+244delinsTCTC MANE Select	NP_066925.1:n.337+241_337+244delinsTCTC
NM_001166103.2:c.166+241_166+244delinsTCTC	NP_001159575.1:n.166+241_166+244delinsTCTC