Canonical Allele Identifier: CA1590312626

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027833G= , CM000667.2:g.149027833G=	GRCh38
NC_000005.9:g.148407396G= , CM000667.1:g.148407396G=	GRCh37
NC_000005.8:g.148387589G=	NCBI36
NG_007947.2:g.40342C= , LRG_269:g.40342C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1795C=
ENST00000515425.6:c.1899C= MANE Select	ENSP00000423660.1:p.Ala633=
ENST00000675793.1:c.*1183C=	ENSP00000502039.1:n.*1183C=
ENST00000676056.1:c.*1409C=	ENSP00000501827.1:n.*1409C=
ENST00000323829.9:c.*1287C=	ENSP00000313025.5:n.*1287C=
ENST00000504517.5:c.1429C=	ENSP00000421779.1:n.1429C=
ENST00000504690.5:c.1899C=	ENSP00000425627.1:p.Ala633=
ENST00000510779.1:c.949C=
ENST00000511307.5:c.*1679C=	ENSP00000421420.1:n.*1679C=
ENST00000512049.5:c.1878C=	ENSP00000421860.1:p.Ala626=
ENST00000513604.5:c.*1287C=	ENSP00000423111.1:n.*1287C=
ENST00000515425.5:c.1899C=	ENSP00000423660.1:p.Ala633=
NM_024577.3:c.1899C= , LRG_269t1:c.1899C=	NP_078853.2:p.Ala633=
NM_024577.4:c.1899C= MANE Select	NP_078853.2:p.Ala633=