Canonical Allele Identifier: CA1590317323

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149038376C= , CM000667.2:g.149038376C=	GRCh38
NC_000005.9:g.148417939C= , CM000667.1:g.148417939C=	GRCh37
NC_000005.8:g.148398132C=	NCBI36
NG_007947.2:g.29799G= , LRG_269:g.29799G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.810G=
ENST00000515425.6:c.920G= MANE Select	ENSP00000423660.1:p.Trp307=
ENST00000674655.1:c.182G=	ENSP00000502840.1:p.Trp61=
ENST00000674983.1:c.*178G=	ENSP00000502387.1:n.*178G=
ENST00000675793.1:c.920G=	ENSP00000502039.1:p.Trp307=
ENST00000676056.1:c.*178G=	ENSP00000501827.1:n.*178G=
ENST00000323829.9:c.*178G=	ENSP00000313025.5:n.*178G=
ENST00000503071.1:n.387G=
ENST00000504517.5:c.320G=	ENSP00000421779.1:p.Trp107=
ENST00000504690.5:c.920G=	ENSP00000425627.1:p.Trp307=
ENST00000511307.5:c.*700G=	ENSP00000421420.1:n.*700G=
ENST00000512049.5:c.899G=	ENSP00000421860.1:p.Trp300=
ENST00000513604.5:c.*178G=	ENSP00000423111.1:n.*178G=
ENST00000515425.5:c.920G=	ENSP00000423660.1:p.Trp307=
NM_024577.3:c.920G= , LRG_269t1:c.920G=	NP_078853.2:p.Trp307=
NM_024577.4:c.920G= MANE Select	NP_078853.2:p.Trp307=