Canonical Allele Identifier: CA1590312059

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026574G= , CM000667.2:g.149026574G=	GRCh38
NC_000005.9:g.148406137G= , CM000667.1:g.148406137G=	GRCh37
NC_000005.8:g.148386330G=	NCBI36
NG_007947.2:g.41601C= , LRG_269:g.41601C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2947C=
ENST00000515425.6:c.3051C= MANE Select	ENSP00000423660.1:p.Ala1017=
ENST00000675793.1:c.*2335C=	ENSP00000502039.1:n.*2335C=
ENST00000676056.1:c.*2561C=	ENSP00000501827.1:n.*2561C=
ENST00000323829.9:c.*2439C=	ENSP00000313025.5:n.*2439C=
ENST00000504517.5:c.2581C=	ENSP00000421779.1:n.2581C=
ENST00000504690.5:c.3051C=	ENSP00000425627.1:p.Ala1017=
ENST00000510779.1:c.2101C=
ENST00000511307.5:c.*2938C=	ENSP00000421420.1:n.*2938C=
ENST00000512049.5:c.3030C=	ENSP00000421860.1:p.Ala1010=
ENST00000513604.5:c.*2546C=	ENSP00000423111.1:n.*2546C=
ENST00000515425.5:c.3051C=	ENSP00000423660.1:p.Ala1017=
NM_024577.3:c.3051C= , LRG_269t1:c.3051C=	NP_078853.2:p.Ala1017=
NM_024577.4:c.3051C= MANE Select	NP_078853.2:p.Ala1017=