Canonical Allele Identifier: CA1590312102

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026674T= , CM000667.2:g.149026674T=	GRCh38
NC_000005.9:g.148406237T= , CM000667.1:g.148406237T=	GRCh37
NC_000005.8:g.148386430T=	NCBI36
NG_007947.2:g.41501A= , LRG_269:g.41501A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2847A=
ENST00000515425.6:c.2951A= MANE Select	ENSP00000423660.1:p.His984=
ENST00000675793.1:c.*2235A=	ENSP00000502039.1:n.*2235A=
ENST00000676056.1:c.*2461A=	ENSP00000501827.1:n.*2461A=
ENST00000323829.9:c.*2339A=	ENSP00000313025.5:n.*2339A=
ENST00000504517.5:c.2481A=	ENSP00000421779.1:n.2481A=
ENST00000504690.5:c.2951A=	ENSP00000425627.1:p.His984=
ENST00000510779.1:c.2001A=
ENST00000511307.5:c.*2838A=	ENSP00000421420.1:n.*2838A=
ENST00000512049.5:c.2930A=	ENSP00000421860.1:p.His977=
ENST00000513604.5:c.*2446A=	ENSP00000423111.1:n.*2446A=
ENST00000515425.5:c.2951A=	ENSP00000423660.1:p.His984=
NM_024577.3:c.2951A= , LRG_269t1:c.2951A=	NP_078853.2:p.His984=
NM_024577.4:c.2951A= MANE Select	NP_078853.2:p.His984=