Canonical Allele Identifier: CA447399455

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149027775-G-A
• MyVariant Identifiers: chr5:g.148407338G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027775G>A , CM000667.2:g.149027775G>A	GRCh38
NC_000005.9:g.148407338G>A , CM000667.1:g.148407338G>A	GRCh37
NC_000005.8:g.148387531G>A	NCBI36
NG_007947.2:g.40400C>T , LRG_269:g.40400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.1853C>T
ENST00000515425.6:c.1957C>T MANE Select	ENSP00000423660.1:p.Leu653=
ENST00000675793.1:c.*1241C>T	ENSP00000502039.1:n.*1241C>T
ENST00000676056.1:c.*1467C>T	ENSP00000501827.1:n.*1467C>T
ENST00000323829.9:c.*1345C>T	ENSP00000313025.5:n.*1345C>T
ENST00000504517.5:c.1487C>T	ENSP00000421779.1:n.1487C>T
ENST00000504690.5:c.1957C>T	ENSP00000425627.1:p.Leu653=
ENST00000510779.1:c.1007C>T
ENST00000511307.5:c.*1737C>T	ENSP00000421420.1:n.*1737C>T
ENST00000512049.5:c.1936C>T	ENSP00000421860.1:p.Leu646=
ENST00000513604.5:c.*1345C>T	ENSP00000423111.1:n.*1345C>T
ENST00000515425.5:c.1957C>T	ENSP00000423660.1:p.Leu653=
NM_024577.3:c.1957C>T , LRG_269t1:c.1957C>T	NP_078853.2:p.Leu653=
NM_024577.4:c.1957C>T MANE Select	NP_078853.2:p.Leu653=