Canonical Allele Identifier: CA1590312135

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026752C= , CM000667.2:g.149026752C=	GRCh38
NC_000005.9:g.148406315C= , CM000667.1:g.148406315C=	GRCh37
NC_000005.8:g.148386508C=	NCBI36
NG_007947.2:g.41423G= , LRG_269:g.41423G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2769G=
ENST00000515425.6:c.2873G= MANE Select	ENSP00000423660.1:p.Ser958=
ENST00000675793.1:c.*2157G=	ENSP00000502039.1:n.*2157G=
ENST00000676056.1:c.*2383G=	ENSP00000501827.1:n.*2383G=
ENST00000323829.9:c.*2261G=	ENSP00000313025.5:n.*2261G=
ENST00000504517.5:c.2403G=	ENSP00000421779.1:n.2403G=
ENST00000504690.5:c.2873G=	ENSP00000425627.1:p.Ser958=
ENST00000510779.1:c.1923G=
ENST00000511307.5:c.*2760G=	ENSP00000421420.1:n.*2760G=
ENST00000512049.5:c.2852G=	ENSP00000421860.1:p.Ser951=
ENST00000513604.5:c.*2368G=	ENSP00000423111.1:n.*2368G=
ENST00000515425.5:c.2873G=	ENSP00000423660.1:p.Ser958=
NM_024577.3:c.2873G= , LRG_269t1:c.2873G=	NP_078853.2:p.Ser958=
NM_024577.4:c.2873G= MANE Select	NP_078853.2:p.Ser958=