Canonical Allele Identifier: CA1590312283

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027090T= , CM000667.2:g.149027090T=	GRCh38
NC_000005.9:g.148406653T= , CM000667.1:g.148406653T=	GRCh37
NC_000005.8:g.148386846T=	NCBI36
NG_007947.2:g.41085A= , LRG_269:g.41085A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2538A=
ENST00000515425.6:c.2642A= MANE Select	ENSP00000423660.1:p.Asn881=
ENST00000675793.1:c.*1926A=	ENSP00000502039.1:n.*1926A=
ENST00000676056.1:c.*2152A=	ENSP00000501827.1:n.*2152A=
ENST00000323829.9:c.*2030A=	ENSP00000313025.5:n.*2030A=
ENST00000504517.5:c.2172A=	ENSP00000421779.1:n.2172A=
ENST00000504690.5:c.2642A=	ENSP00000425627.1:p.Asn881=
ENST00000510779.1:c.1692A=
ENST00000511307.5:c.*2422A=	ENSP00000421420.1:n.*2422A=
ENST00000512049.5:c.2621A=	ENSP00000421860.1:p.Asn874=
ENST00000513604.5:c.*2030A=	ENSP00000423111.1:n.*2030A=
ENST00000515425.5:c.2642A=	ENSP00000423660.1:p.Asn881=
NM_024577.3:c.2642A= , LRG_269t1:c.2642A=	NP_078853.2:p.Asn881=
NM_024577.4:c.2642A= MANE Select	NP_078853.2:p.Asn881=