Canonical Allele Identifier: CA1590312546

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027673G= , CM000667.2:g.149027673G=	GRCh38
NC_000005.9:g.148407236G= , CM000667.1:g.148407236G=	GRCh37
NC_000005.8:g.148387429G=	NCBI36
NG_007947.2:g.40502C= , LRG_269:g.40502C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1955C=
ENST00000515425.6:c.2059C= MANE Select	ENSP00000423660.1:p.His687=
ENST00000675793.1:c.*1343C=	ENSP00000502039.1:n.*1343C=
ENST00000676056.1:c.*1569C=	ENSP00000501827.1:n.*1569C=
ENST00000323829.9:c.*1447C=	ENSP00000313025.5:n.*1447C=
ENST00000504517.5:c.1589C=	ENSP00000421779.1:n.1589C=
ENST00000504690.5:c.2059C=	ENSP00000425627.1:p.His687=
ENST00000510779.1:c.1109C=
ENST00000511307.5:c.*1839C=	ENSP00000421420.1:n.*1839C=
ENST00000512049.5:c.2038C=	ENSP00000421860.1:p.His680=
ENST00000513604.5:c.*1447C=	ENSP00000423111.1:n.*1447C=
ENST00000515425.5:c.2059C=	ENSP00000423660.1:p.His687=
NM_024577.3:c.2059C= , LRG_269t1:c.2059C=	NP_078853.2:p.His687=
NM_024577.4:c.2059C= MANE Select	NP_078853.2:p.His687=