Canonical Allele Identifier: CA1590312099

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026669G= , CM000667.2:g.149026669G=	GRCh38
NC_000005.9:g.148406232G= , CM000667.1:g.148406232G=	GRCh37
NC_000005.8:g.148386425G=	NCBI36
NG_007947.2:g.41506C= , LRG_269:g.41506C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2852C=
ENST00000515425.6:c.2956C= MANE Select	ENSP00000423660.1:p.His986=
ENST00000675793.1:c.*2240C=	ENSP00000502039.1:n.*2240C=
ENST00000676056.1:c.*2466C=	ENSP00000501827.1:n.*2466C=
ENST00000323829.9:c.*2344C=	ENSP00000313025.5:n.*2344C=
ENST00000504517.5:c.2486C=	ENSP00000421779.1:n.2486C=
ENST00000504690.5:c.2956C=	ENSP00000425627.1:p.His986=
ENST00000510779.1:c.2006C=
ENST00000511307.5:c.*2843C=	ENSP00000421420.1:n.*2843C=
ENST00000512049.5:c.2935C=	ENSP00000421860.1:p.His979=
ENST00000513604.5:c.*2451C=	ENSP00000423111.1:n.*2451C=
ENST00000515425.5:c.2956C=	ENSP00000423660.1:p.His986=
NM_024577.3:c.2956C= , LRG_269t1:c.2956C=	NP_078853.2:p.His986=
NM_024577.4:c.2956C= MANE Select	NP_078853.2:p.His986=