Canonical Allele Identifier: CA447399342

Gene: SH3TC2

Linked Data

• MyVariant Identifiers: chr5:g.148407114T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149027551T>G , CM000667.2:g.149027551T>G	GRCh38
NC_000005.9:g.148407114T>G , CM000667.1:g.148407114T>G	GRCh37
NC_000005.8:g.148387307T>G	NCBI36
NG_007947.2:g.40624A>C , LRG_269:g.40624A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.2077A>C
ENST00000515425.6:c.2181A>C MANE Select	ENSP00000423660.1:p.Pro727=
ENST00000675793.1:c.*1465A>C	ENSP00000502039.1:n.*1465A>C
ENST00000676056.1:c.*1691A>C	ENSP00000501827.1:n.*1691A>C
ENST00000323829.9:c.*1569A>C	ENSP00000313025.5:n.*1569A>C
ENST00000504517.5:c.1711A>C	ENSP00000421779.1:n.1711A>C
ENST00000504690.5:c.2181A>C	ENSP00000425627.1:p.Pro727=
ENST00000510779.1:c.1231A>C
ENST00000511307.5:c.*1961A>C	ENSP00000421420.1:n.*1961A>C
ENST00000512049.5:c.2160A>C	ENSP00000421860.1:p.Pro720=
ENST00000513604.5:c.*1569A>C	ENSP00000423111.1:n.*1569A>C
ENST00000515425.5:c.2181A>C	ENSP00000423660.1:p.Pro727=
NM_024577.3:c.2181A>C , LRG_269t1:c.2181A>C	NP_078853.2:p.Pro727=
NM_024577.4:c.2181A>C MANE Select	NP_078853.2:p.Pro727=