Canonical Allele Identifier: CA361666917

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149027558-G-A
• COSMIC: COSM5918807 ; COSM5918808
• MyVariant Identifiers: chr5:g.148407121G>A (hg19) ; chr5:g.149027558G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027558G>A , CM000667.2:g.149027558G>A	GRCh38
NC_000005.9:g.148407121G>A , CM000667.1:g.148407121G>A	GRCh37
NC_000005.8:g.148387314G>A	NCBI36
NG_007947.2:g.40617C>T , LRG_269:g.40617C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2070C>T
ENST00000515425.6:c.2174C>T MANE Select	ENSP00000423660.1:p.Pro725Leu
ENST00000675793.1:c.*1458C>T	ENSP00000502039.1:n.*1458C>T
ENST00000676056.1:c.*1684C>T	ENSP00000501827.1:n.*1684C>T
ENST00000323829.9:c.*1562C>T	ENSP00000313025.5:n.*1562C>T
ENST00000504517.5:c.1704C>T	ENSP00000421779.1:n.1704C>T
ENST00000504690.5:c.2174C>T	ENSP00000425627.1:p.Pro725Leu
ENST00000510779.1:c.1224C>T
ENST00000511307.5:c.*1954C>T	ENSP00000421420.1:n.*1954C>T
ENST00000512049.5:c.2153C>T	ENSP00000421860.1:p.Pro718Leu
ENST00000513604.5:c.*1562C>T	ENSP00000423111.1:n.*1562C>T
ENST00000515425.5:c.2174C>T	ENSP00000423660.1:p.Pro725Leu
NM_024577.3:c.2174C>T , LRG_269t1:c.2174C>T	NP_078853.2:p.Pro725Leu
NM_024577.4:c.2174C>T MANE Select	NP_078853.2:p.Pro725Leu