Canonical Allele Identifier: CA1590312040

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026530G= , CM000667.2:g.149026530G=	GRCh38
NC_000005.9:g.148406093G= , CM000667.1:g.148406093G=	GRCh37
NC_000005.8:g.148386286G=	NCBI36
NG_007947.2:g.41645C= , LRG_269:g.41645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2949+42C=
ENST00000515425.6:c.3053+42C= MANE Select	ENSP00000423660.1:n.3053+42C=
ENST00000675793.1:c.*2337+42C=	ENSP00000502039.1:n.*2337+42C=
ENST00000676056.1:c.*2563+42C=	ENSP00000501827.1:n.*2563+42C=
ENST00000323829.9:c.*2441+42C=	ENSP00000313025.5:n.*2441+42C=
ENST00000504517.5:c.2583+42C=	ENSP00000421779.1:n.2583+42C=
ENST00000504690.5:c.3053+42C=	ENSP00000425627.1:n.3053+42C=
ENST00000510779.1:c.2103+42C=
ENST00000512049.5:c.3032+42C=	ENSP00000421860.1:n.3032+42C=
ENST00000513604.5:c.*2590C=	ENSP00000423111.1:n.*2590C=
ENST00000515425.5:c.3053+42C=	ENSP00000423660.1:n.3053+42C=
NM_024577.3:c.3053+42C= , LRG_269t1:c.3053+42C=	NP_078853.2:n.3053+42C=
NM_024577.4:c.3053+42C= MANE Select	NP_078853.2:n.3053+42C=