Canonical Allele Identifier: CA1590312091

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026654C= , CM000667.2:g.149026654C=	GRCh38
NC_000005.9:g.148406217C= , CM000667.1:g.148406217C=	GRCh37
NC_000005.8:g.148386410C=	NCBI36
NG_007947.2:g.41521G= , LRG_269:g.41521G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2867G=
ENST00000515425.6:c.2971G= MANE Select	ENSP00000423660.1:p.Ala991=
ENST00000675793.1:c.*2255G=	ENSP00000502039.1:n.*2255G=
ENST00000676056.1:c.*2481G=	ENSP00000501827.1:n.*2481G=
ENST00000323829.9:c.*2359G=	ENSP00000313025.5:n.*2359G=
ENST00000504517.5:c.2501G=	ENSP00000421779.1:n.2501G=
ENST00000504690.5:c.2971G=	ENSP00000425627.1:p.Ala991=
ENST00000510779.1:c.2021G=
ENST00000511307.5:c.*2858G=	ENSP00000421420.1:n.*2858G=
ENST00000512049.5:c.2950G=	ENSP00000421860.1:p.Ala984=
ENST00000513604.5:c.*2466G=	ENSP00000423111.1:n.*2466G=
ENST00000515425.5:c.2971G=	ENSP00000423660.1:p.Ala991=
NM_024577.3:c.2971G= , LRG_269t1:c.2971G=	NP_078853.2:p.Ala991=
NM_024577.4:c.2971G= MANE Select	NP_078853.2:p.Ala991=