Canonical Allele Identifier: CA361667109

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407208T>G (hg19) ; chr5:g.149027645T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027645T>G , CM000667.2:g.149027645T>G	GRCh38
NC_000005.9:g.148407208T>G , CM000667.1:g.148407208T>G	GRCh37
NC_000005.8:g.148387401T>G	NCBI36
NG_007947.2:g.40530A>C , LRG_269:g.40530A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1983A>C
ENST00000515425.6:c.2087A>C MANE Select	ENSP00000423660.1:p.His696Pro
ENST00000675793.1:c.*1371A>C	ENSP00000502039.1:n.*1371A>C
ENST00000676056.1:c.*1597A>C	ENSP00000501827.1:n.*1597A>C
ENST00000323829.9:c.*1475A>C	ENSP00000313025.5:n.*1475A>C
ENST00000504517.5:c.1617A>C	ENSP00000421779.1:n.1617A>C
ENST00000504690.5:c.2087A>C	ENSP00000425627.1:p.His696Pro
ENST00000510779.1:c.1137A>C
ENST00000511307.5:c.*1867A>C	ENSP00000421420.1:n.*1867A>C
ENST00000512049.5:c.2066A>C	ENSP00000421860.1:p.His689Pro
ENST00000513604.5:c.*1475A>C	ENSP00000423111.1:n.*1475A>C
ENST00000515425.5:c.2087A>C	ENSP00000423660.1:p.His696Pro
NM_024577.3:c.2087A>C , LRG_269t1:c.2087A>C	NP_078853.2:p.His696Pro
NM_024577.4:c.2087A>C MANE Select	NP_078853.2:p.His696Pro