Canonical Allele Identifier: CA1590312197

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026872_149026874delinsGAT , CM000667.2:g.149026872_149026874delinsGAT	GRCh38
NC_000005.9:g.148406435_148406437delinsGAT , CM000667.1:g.148406435_148406437delinsGAT	GRCh37
NC_000005.8:g.148386628_148386630delinsGAT	NCBI36
NG_007947.2:g.41301_41303delinsATC , LRG_269:g.41301_41303delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2754_2756delinsATC
ENST00000515425.6:c.2858_2860delinsATC MANE Select	ENSP00000423660.1:p.His953=
ENST00000675793.1:c.*2142_*2144delinsATC	ENSP00000502039.1:n.*2142_*2144delinsATC
ENST00000676056.1:c.*2368_*2370delinsATC	ENSP00000501827.1:n.*2368_*2370delinsATC
ENST00000323829.9:c.*2246_*2248delinsATC	ENSP00000313025.5:n.*2246_*2248delinsATC
ENST00000504517.5:c.2388_2390delinsATC	ENSP00000421779.1:n.2388_2390delinsATC
ENST00000504690.5:c.2858_2860delinsATC	ENSP00000425627.1:p.His953=
ENST00000510779.1:c.1908_1910delinsATC
ENST00000511307.5:c.*2638_*2640delinsATC	ENSP00000421420.1:n.*2638_*2640delinsATC
ENST00000512049.5:c.2837_2839delinsATC	ENSP00000421860.1:p.His946=
ENST00000513604.5:c.*2246_*2248delinsATC	ENSP00000423111.1:n.*2246_*2248delinsATC
ENST00000515425.5:c.2858_2860delinsATC	ENSP00000423660.1:p.His953=
NM_024577.3:c.2858_2860delinsATC , LRG_269t1:c.2858_2860delinsATC	NP_078853.2:p.His953=
NM_024577.4:c.2858_2860delinsATC MANE Select	NP_078853.2:p.His953=