Canonical Allele Identifier: CA405631653

Gene: SPINT2

Linked Data

• MyVariant Identifiers: chr19:g.38778540C>G (hg19) ; chr19:g.38287900C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287900C>G , CM000681.2:g.38287900C>G	GRCh38
NC_000019.9:g.38778540C>G , CM000681.1:g.38778540C>G	GRCh37
NC_000019.8:g.43470380C>G	NCBI36
NG_013372.1:g.28443C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.302C>G MANE Select	ENSP00000301244.5:p.Thr101Ser
ENST00000301244.11:c.302C>G	ENSP00000301244.5:p.Thr101Ser
ENST00000454580.7:c.131C>G	ENSP00000389788.2:p.Thr44Ser
ENST00000587090.5:c.152C>G	ENSP00000466407.1:p.Thr51Ser
ENST00000587516.5:c.278-1238C>G	ENSP00000465721.1:n.278-1238C>G
ENST00000590210.1:n.499C>G
ENST00000590510.5:c.152C>G	ENSP00000465301.1:p.Thr51Ser
ENST00000592007.1:c.152C>G	ENSP00000465561.1:p.Thr51Ser
NM_001166103.1:c.131C>G	NP_001159575.1:p.Thr44Ser
NM_021102.3:c.302C>G	NP_066925.1:p.Thr101Ser
NM_021102.4:c.302C>G MANE Select	NP_066925.1:p.Thr101Ser
NM_001166103.2:c.131C>G	NP_001159575.1:p.Thr44Ser