Canonical Allele Identifier: CA3499118

Gene: SH3TC2

Linked Data

• ClinVar Variation Id: 694975
• ClinVar RCV Id: RCV000857150 ; RCV001300966 ; RCV002409010
• dbSNP Id: rs778936762
• ExAC: 5:148407482 G / A
• gnomAD v2: 5-148407482-G-A
• gnomAD v3: 5-149027919-G-A
• gnomAD v4: 5-149027919-G-A
• MyVariant Identifiers: chr5:g.148407482G>A (hg19) ; chr5:g.149027919G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027919G>A , CM000667.2:g.149027919G>A	GRCh38
NC_000005.9:g.148407482G>A , CM000667.1:g.148407482G>A	GRCh37
NC_000005.8:g.148387675G>A	NCBI36
NG_007947.2:g.40256C>T , LRG_269:g.40256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1709C>T
ENST00000515425.6:c.1813C>T MANE Select	ENSP00000423660.1:p.Arg605Cys
ENST00000675793.1:c.*1097C>T	ENSP00000502039.1:n.*1097C>T
ENST00000676056.1:c.*1323C>T	ENSP00000501827.1:n.*1323C>T
ENST00000323829.9:c.*1201C>T	ENSP00000313025.5:n.*1201C>T
ENST00000504517.5:c.1343C>T	ENSP00000421779.1:n.1343C>T
ENST00000504690.5:c.1813C>T	ENSP00000425627.1:p.Arg605Cys
ENST00000510779.1:c.863C>T
ENST00000511307.5:c.*1593C>T	ENSP00000421420.1:n.*1593C>T
ENST00000512049.5:c.1792C>T	ENSP00000421860.1:p.Arg598Cys
ENST00000513604.5:c.*1201C>T	ENSP00000423111.1:n.*1201C>T
ENST00000515425.5:c.1813C>T	ENSP00000423660.1:p.Arg605Cys
NM_024577.3:c.1813C>T , LRG_269t1:c.1813C>T	NP_078853.2:p.Arg605Cys
NM_024577.4:c.1813C>T MANE Select	NP_078853.2:p.Arg605Cys