Canonical Allele Identifier: CA1590312161

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026797A= , CM000667.2:g.149026797A=	GRCh38
NC_000005.9:g.148406360A= , CM000667.1:g.148406360A=	GRCh37
NC_000005.8:g.148386553A=	NCBI36
NG_007947.2:g.41378T= , LRG_269:g.41378T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2769-45T=
ENST00000515425.6:c.2873-45T= MANE Select	ENSP00000423660.1:n.2873-45T=
ENST00000675793.1:c.*2157-45T=	ENSP00000502039.1:n.*2157-45T=
ENST00000676056.1:c.*2383-45T=	ENSP00000501827.1:n.*2383-45T=
ENST00000323829.9:c.*2261-45T=	ENSP00000313025.5:n.*2261-45T=
ENST00000504517.5:c.2403-45T=	ENSP00000421779.1:n.2403-45T=
ENST00000504690.5:c.2873-45T=	ENSP00000425627.1:n.2873-45T=
ENST00000510779.1:c.1923-45T=
ENST00000511307.5:c.*2715T=	ENSP00000421420.1:n.*2715T=
ENST00000512049.5:c.2852-45T=	ENSP00000421860.1:n.2852-45T=
ENST00000513604.5:c.*2323T=	ENSP00000423111.1:n.*2323T=
ENST00000515425.5:c.2873-45T=	ENSP00000423660.1:n.2873-45T=
NM_024577.3:c.2873-45T= , LRG_269t1:c.2873-45T=	NP_078853.2:n.2873-45T=
NM_024577.4:c.2873-45T= MANE Select	NP_078853.2:n.2873-45T=