Canonical Allele Identifier: CA1590304264

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008982G= , CM000667.2:g.149008982G=	GRCh38
NC_000005.9:g.148388545G= , CM000667.1:g.148388545G=	GRCh37
NC_000005.8:g.148368738G=	NCBI36
NG_007947.2:g.59193C= , LRG_269:g.59193C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3243C=
ENST00000515425.6:c.3347C= MANE Select	ENSP00000423660.1:p.Ala1116=
ENST00000675793.1:c.*2631C=	ENSP00000502039.1:n.*2631C=
ENST00000323829.9:c.*2735C=	ENSP00000313025.5:n.*2735C=
ENST00000504517.5:c.2877C=	ENSP00000421779.1:n.2877C=
ENST00000504690.5:c.3347C=	ENSP00000425627.1:p.Ala1116=
ENST00000510779.1:c.2397C=
ENST00000512049.5:c.3326C=	ENSP00000421860.1:p.Ala1109=
ENST00000515229.5:n.9C=
ENST00000515425.5:c.3347C=	ENSP00000423660.1:p.Ala1116=
NM_024577.3:c.3347C= , LRG_269t1:c.3347C=	NP_078853.2:p.Ala1116=
NM_024577.4:c.3347C= MANE Select	NP_078853.2:p.Ala1116=