Canonical Allele Identifier: CA1590328052

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149062793_149062794delinsCT , CM000667.2:g.149062793_149062794delinsCT	GRCh38
NC_000005.9:g.148442356_148442357delinsCT , CM000667.1:g.148442356_148442357delinsCT	GRCh37
NC_000005.8:g.148422549_148422550delinsCT	NCBI36
NG_007947.2:g.5381_5382delinsAG , LRG_269:g.5381_5382delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515425.6:c.52+177_52+178delinsAG MANE Select	ENSP00000423660.1:n.52+177_52+178delinsAG
ENST00000674983.1:c.52+177_52+178delinsAG	ENSP00000502387.1:n.52+177_52+178delinsAG
ENST00000675793.1:c.52+177_52+178delinsAG	ENSP00000502039.1:n.52+177_52+178delinsAG
ENST00000676056.1:c.52+177_52+178delinsAG	ENSP00000501827.1:n.52+177_52+178delinsAG
ENST00000323829.9:c.52+177_52+178delinsAG	ENSP00000313025.5:n.52+177_52+178delinsAG
ENST00000504091.1:n.88+177_88+178delinsAG
ENST00000504690.5:c.52+177_52+178delinsAG	ENSP00000425627.1:n.52+177_52+178delinsAG
ENST00000511307.5:c.52+177_52+178delinsAG	ENSP00000421420.1:n.52+177_52+178delinsAG
ENST00000511949.5:n.92+177_92+178delinsAG
ENST00000512049.5:c.52+177_52+178delinsAG	ENSP00000421860.1:n.52+177_52+178delinsAG
ENST00000513604.5:c.52+177_52+178delinsAG	ENSP00000423111.1:n.52+177_52+178delinsAG
ENST00000515425.5:c.52+177_52+178delinsAG	ENSP00000423660.1:n.52+177_52+178delinsAG
NM_024577.3:c.52+177_52+178delinsAG , LRG_269t1:c.52+177_52+178delinsAG	NP_078853.2:n.52+177_52+178delinsAG
NM_024577.4:c.52+177_52+178delinsAG MANE Select	NP_078853.2:n.52+177_52+178delinsAG