Canonical Allele Identifier: CA361665800

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027022G>C , CM000667.2:g.149027022G>C	GRCh38
NC_000005.9:g.148406585G>C , CM000667.1:g.148406585G>C	GRCh37
NC_000005.8:g.148386778G>C	NCBI36
NG_007947.2:g.41153C>G , LRG_269:g.41153C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_024577.4:c.2710C>G MANE Select	NP_078853.2:p.Arg904Gly
ENST00000515425.6:c.2710C>G MANE Select	ENSP00000423660.1:p.Arg904Gly
NM_024577.3:c.2710C>G , LRG_269t1:c.2710C>G	NP_078853.2:p.Arg904Gly
ENST00000323829.9:c.*2098C>G	ENSP00000313025.5:n.*2098C>G
ENST00000502274.2:c.2606C>G
ENST00000504517.5:c.2240C>G	ENSP00000421779.1:n.2240C>G
ENST00000504690.5:c.2710C>G	ENSP00000425627.1:p.Arg904Gly
ENST00000510779.1:c.1760C>G
ENST00000511307.5:c.*2490C>G	ENSP00000421420.1:n.*2490C>G
ENST00000512049.5:c.2689C>G	ENSP00000421860.1:p.Arg897Gly
ENST00000513604.5:c.*2098C>G	ENSP00000423111.1:n.*2098C>G
ENST00000515425.5:c.2710C>G	ENSP00000423660.1:p.Arg904Gly
ENST00000675793.1:c.*1994C>G	ENSP00000502039.1:n.*1994C>G
ENST00000676056.1:c.*2220C>G	ENSP00000501827.1:n.*2220C>G