Canonical Allele Identifier: CA361667350

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407324C>G (hg19) ; chr5:g.149027761C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027761C>G , CM000667.2:g.149027761C>G	GRCh38
NC_000005.9:g.148407324C>G , CM000667.1:g.148407324C>G	GRCh37
NC_000005.8:g.148387517C>G	NCBI36
NG_007947.2:g.40414G>C , LRG_269:g.40414G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1867G>C
ENST00000515425.6:c.1971G>C MANE Select	ENSP00000423660.1:p.Glu657Asp
ENST00000675793.1:c.*1255G>C	ENSP00000502039.1:n.*1255G>C
ENST00000676056.1:c.*1481G>C	ENSP00000501827.1:n.*1481G>C
ENST00000323829.9:c.*1359G>C	ENSP00000313025.5:n.*1359G>C
ENST00000504517.5:c.1501G>C	ENSP00000421779.1:n.1501G>C
ENST00000504690.5:c.1971G>C	ENSP00000425627.1:p.Glu657Asp
ENST00000510779.1:c.1021G>C
ENST00000511307.5:c.*1751G>C	ENSP00000421420.1:n.*1751G>C
ENST00000512049.5:c.1950G>C	ENSP00000421860.1:p.Glu650Asp
ENST00000513604.5:c.*1359G>C	ENSP00000423111.1:n.*1359G>C
ENST00000515425.5:c.1971G>C	ENSP00000423660.1:p.Glu657Asp
NM_024577.3:c.1971G>C , LRG_269t1:c.1971G>C	NP_078853.2:p.Glu657Asp
NM_024577.4:c.1971G>C MANE Select	NP_078853.2:p.Glu657Asp