Canonical Allele Identifier: CA2675887480

Gene: SH3TC2

Linked Data

• gnomAD v4: 5-149026549-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149026549G>T , CM000667.2:g.149026549G>T	GRCh38
NC_000005.9:g.148406112G>T , CM000667.1:g.148406112G>T	GRCh37
NC_000005.8:g.148386305G>T	NCBI36
NG_007947.2:g.41626C>A , LRG_269:g.41626C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.2949+23C>A
ENST00000515425.6:c.3053+23C>A MANE Select	ENSP00000423660.1:n.3053+23C>A
ENST00000675793.1:c.*2337+23C>A	ENSP00000502039.1:n.*2337+23C>A
ENST00000676056.1:c.*2563+23C>A	ENSP00000501827.1:n.*2563+23C>A
ENST00000323829.9:c.*2441+23C>A	ENSP00000313025.5:n.*2441+23C>A
ENST00000504517.5:c.2583+23C>A	ENSP00000421779.1:n.2583+23C>A
ENST00000504690.5:c.3053+23C>A	ENSP00000425627.1:n.3053+23C>A
ENST00000510779.1:c.2103+23C>A
ENST00000512049.5:c.3032+23C>A	ENSP00000421860.1:n.3032+23C>A
ENST00000513604.5:c.*2571C>A	ENSP00000423111.1:n.*2571C>A
ENST00000515425.5:c.3053+23C>A	ENSP00000423660.1:n.3053+23C>A
NM_024577.3:c.3053+23C>A , LRG_269t1:c.3053+23C>A	NP_078853.2:n.3053+23C>A
NM_024577.4:c.3053+23C>A MANE Select	NP_078853.2:n.3053+23C>A