Canonical Allele Identifier: CA1590303404

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149007053G= , CM000667.2:g.149007053G=	GRCh38
NC_000005.9:g.148386616G= , CM000667.1:g.148386616G=	GRCh37
NC_000005.8:g.148366809G=	NCBI36
NG_007947.2:g.61122C= , LRG_269:g.61122C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.4356C=
ENST00000515425.6:c.3503C= MANE Select	ENSP00000423660.1:p.Ala1168=
ENST00000675793.1:c.*4560C=	ENSP00000502039.1:n.*4560C=
ENST00000323829.9:c.*2891C=	ENSP00000313025.5:n.*2891C=
ENST00000502274.1:c.89C=	ENSP00000421092.1:p.Ala30=
ENST00000504517.5:c.3025C=	ENSP00000421779.1:n.3025C=
ENST00000504690.5:c.3503C=	ENSP00000425627.1:p.Ala1168=
ENST00000510350.1:n.59C=
ENST00000510779.1:c.2553C=
ENST00000512049.5:c.3482C=	ENSP00000421860.1:p.Ala1161=
ENST00000515229.5:n.165C=
ENST00000515425.5:c.3503C=	ENSP00000423660.1:p.Ala1168=
NM_024577.3:c.3503C= , LRG_269t1:c.3503C=	NP_078853.2:p.Ala1168=
NM_024577.4:c.3503C= MANE Select	NP_078853.2:p.Ala1168=