Canonical Allele Identifier: CA361666897

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407109C>G (hg19) ; chr5:g.149027546C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027546C>G , CM000667.2:g.149027546C>G	GRCh38
NC_000005.9:g.148407109C>G , CM000667.1:g.148407109C>G	GRCh37
NC_000005.8:g.148387302C>G	NCBI36
NG_007947.2:g.40629G>C , LRG_269:g.40629G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2082G>C
ENST00000515425.6:c.2186G>C MANE Select	ENSP00000423660.1:p.Trp729Ser
ENST00000675793.1:c.*1470G>C	ENSP00000502039.1:n.*1470G>C
ENST00000676056.1:c.*1696G>C	ENSP00000501827.1:n.*1696G>C
ENST00000323829.9:c.*1574G>C	ENSP00000313025.5:n.*1574G>C
ENST00000504517.5:c.1716G>C	ENSP00000421779.1:n.1716G>C
ENST00000504690.5:c.2186G>C	ENSP00000425627.1:p.Trp729Ser
ENST00000510779.1:c.1236G>C
ENST00000511307.5:c.*1966G>C	ENSP00000421420.1:n.*1966G>C
ENST00000512049.5:c.2165G>C	ENSP00000421860.1:p.Trp722Ser
ENST00000513604.5:c.*1574G>C	ENSP00000423111.1:n.*1574G>C
ENST00000515425.5:c.2186G>C	ENSP00000423660.1:p.Trp729Ser
NM_024577.3:c.2186G>C , LRG_269t1:c.2186G>C	NP_078853.2:p.Trp729Ser
NM_024577.4:c.2186G>C MANE Select	NP_078853.2:p.Trp729Ser