Canonical Allele Identifier: CA361667130

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407218C>T (hg19) ; chr5:g.149027655C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027655C>T , CM000667.2:g.149027655C>T	GRCh38
NC_000005.9:g.148407218C>T , CM000667.1:g.148407218C>T	GRCh37
NC_000005.8:g.148387411C>T	NCBI36
NG_007947.2:g.40520G>A , LRG_269:g.40520G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.1973G>A
ENST00000515425.6:c.2077G>A MANE Select	ENSP00000423660.1:p.Val693Ile
ENST00000675793.1:c.*1361G>A	ENSP00000502039.1:n.*1361G>A
ENST00000676056.1:c.*1587G>A	ENSP00000501827.1:n.*1587G>A
ENST00000323829.9:c.*1465G>A	ENSP00000313025.5:n.*1465G>A
ENST00000504517.5:c.1607G>A	ENSP00000421779.1:n.1607G>A
ENST00000504690.5:c.2077G>A	ENSP00000425627.1:p.Val693Ile
ENST00000510779.1:c.1127G>A
ENST00000511307.5:c.*1857G>A	ENSP00000421420.1:n.*1857G>A
ENST00000512049.5:c.2056G>A	ENSP00000421860.1:p.Val686Ile
ENST00000513604.5:c.*1465G>A	ENSP00000423111.1:n.*1465G>A
ENST00000515425.5:c.2077G>A	ENSP00000423660.1:p.Val693Ile
NM_024577.3:c.2077G>A , LRG_269t1:c.2077G>A	NP_078853.2:p.Val693Ile
NM_024577.4:c.2077G>A MANE Select	NP_078853.2:p.Val693Ile