Canonical Allele Identifier: CA1590314458

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149031551C= , CM000667.2:g.149031551C=	GRCh38
NC_000005.9:g.148411114C= , CM000667.1:g.148411114C=	GRCh37
NC_000005.8:g.148391307C=	NCBI36
NG_007947.2:g.36624G= , LRG_269:g.36624G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024577.4:c.1135+3G= MANE Select	NP_078853.2:n.1135+3G=
ENST00000515425.6:c.1135+3G= MANE Select	ENSP00000423660.1:n.1135+3G=
NM_024577.3:c.1135+3G= , LRG_269t1:c.1135+3G=	NP_078853.2:n.1135+3G=
ENST00000323829.9:c.*523+3G=	ENSP00000313025.5:n.*523+3G=
ENST00000502274.2:c.1155+3G=
ENST00000504517.5:c.665+3G=	ENSP00000421779.1:n.665+3G=
ENST00000504690.5:c.1135+3G=	ENSP00000425627.1:n.1135+3G=
ENST00000510779.1:c.63+3G=
ENST00000511307.5:c.*915+3G=	ENSP00000421420.1:n.*915+3G=
ENST00000512049.5:c.1114+3G=	ENSP00000421860.1:n.1114+3G=
ENST00000513340.1:n.509+3G=
ENST00000513604.5:c.*523+3G=	ENSP00000423111.1:n.*523+3G=
ENST00000515425.5:c.1135+3G=	ENSP00000423660.1:n.1135+3G=
ENST00000675793.1:c.*419+3G=	ENSP00000502039.1:n.*419+3G=
ENST00000676056.1:c.*523+3G=	ENSP00000501827.1:n.*523+3G=