Canonical Allele Identifier: CA1590304091

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008599T= , CM000667.2:g.149008599T=	GRCh38
NC_000005.9:g.148388162T= , CM000667.1:g.148388162T=	GRCh37
NC_000005.8:g.148368355T=	NCBI36
NG_007947.2:g.59576A= , LRG_269:g.59576A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3374+252A=
ENST00000515425.6:c.3478+252A= MANE Select	ENSP00000423660.1:n.3478+252A=
ENST00000675793.1:c.*3014A=	ENSP00000502039.1:n.*3014A=
ENST00000323829.9:c.*2866+252A=	ENSP00000313025.5:n.*2866+252A=
ENST00000502274.1:c.-1458A=	ENSP00000421092.1:n.-1458A=
ENST00000504517.5:c.3008+252A=	ENSP00000421779.1:n.3008+252A=
ENST00000504690.5:c.3478+252A=	ENSP00000425627.1:n.3478+252A=
ENST00000510779.1:c.2528+252A=
ENST00000512049.5:c.3457+252A=	ENSP00000421860.1:n.3457+252A=
ENST00000515229.5:n.140+252A=
ENST00000515425.5:c.3478+252A=	ENSP00000423660.1:n.3478+252A=
NM_024577.3:c.3478+252A= , LRG_269t1:c.3478+252A=	NP_078853.2:n.3478+252A=
NM_024577.4:c.3478+252A= MANE Select	NP_078853.2:n.3478+252A=