Canonical Allele Identifier: CA1590304267

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008987_149008988delinsAG , CM000667.2:g.149008987_149008988delinsAG	GRCh38
NC_000005.9:g.148388550_148388551delinsAG , CM000667.1:g.148388550_148388551delinsAG	GRCh37
NC_000005.8:g.148368743_148368744delinsAG	NCBI36
NG_007947.2:g.59187_59188delinsCT , LRG_269:g.59187_59188delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3237_3238delinsCT
ENST00000515425.6:c.3341_3342delinsCT MANE Select	ENSP00000423660.1:p.Pro1114=
ENST00000675793.1:c.*2625_*2626delinsCT	ENSP00000502039.1:n.*2625_*2626delinsCT
ENST00000323829.9:c.*2729_*2730delinsCT	ENSP00000313025.5:n.*2729_*2730delinsCT
ENST00000504517.5:c.2871_2872delinsCT	ENSP00000421779.1:n.2871_2872delinsCT
ENST00000504690.5:c.3341_3342delinsCT	ENSP00000425627.1:p.Pro1114=
ENST00000510779.1:c.2391_2392delinsCT
ENST00000512049.5:c.3320_3321delinsCT	ENSP00000421860.1:p.Pro1107=
ENST00000515229.5:n.3_4delinsCT
ENST00000515425.5:c.3341_3342delinsCT	ENSP00000423660.1:p.Pro1114=
NM_024577.3:c.3341_3342delinsCT , LRG_269t1:c.3341_3342delinsCT	NP_078853.2:p.Pro1114=
NM_024577.4:c.3341_3342delinsCT MANE Select	NP_078853.2:p.Pro1114=