Canonical Allele Identifier: CA3498923

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026874T>G , CM000667.2:g.149026874T>G	GRCh38
NC_000005.9:g.148406437T>G , CM000667.1:g.148406437T>G	GRCh37
NC_000005.8:g.148386630T>G	NCBI36
NG_007947.2:g.41301A>C , LRG_269:g.41301A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024577.4:c.2858A>C MANE Select	NP_078853.2:p.His953Pro
ENST00000515425.6:c.2858A>C MANE Select	ENSP00000423660.1:p.His953Pro
NM_024577.3:c.2858A>C , LRG_269t1:c.2858A>C	NP_078853.2:p.His953Pro
ENST00000323829.9:c.*2246A>C	ENSP00000313025.5:n.*2246A>C
ENST00000502274.2:c.2754A>C
ENST00000504517.5:c.2388A>C	ENSP00000421779.1:n.2388A>C
ENST00000504690.5:c.2858A>C	ENSP00000425627.1:p.His953Pro
ENST00000510779.1:c.1908A>C
ENST00000511307.5:c.*2638A>C	ENSP00000421420.1:n.*2638A>C
ENST00000512049.5:c.2837A>C	ENSP00000421860.1:p.His946Pro
ENST00000513604.5:c.*2246A>C	ENSP00000423111.1:n.*2246A>C
ENST00000515425.5:c.2858A>C	ENSP00000423660.1:p.His953Pro
ENST00000675793.1:c.*2142A>C	ENSP00000502039.1:n.*2142A>C
ENST00000676056.1:c.*2368A>C	ENSP00000501827.1:n.*2368A>C