Canonical Allele Identifier: CA1590304289

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149009032_149009033delinsTA , CM000667.2:g.149009032_149009033delinsTA	GRCh38
NC_000005.9:g.148388595_148388596delinsTA , CM000667.1:g.148388595_148388596delinsTA	GRCh37
NC_000005.8:g.148368788_148368789delinsTA	NCBI36
NG_007947.2:g.59142_59143delinsTA , LRG_269:g.59142_59143delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3224-32_3224-31delinsTA
ENST00000515425.6:c.3328-32_3328-31delinsTA MANE Select	ENSP00000423660.1:n.3328-32_3328-31delinsTA
ENST00000675793.1:c.*2612-32_*2612-31delinsTA	ENSP00000502039.1:n.*2612-32_*2612-31delinsTA
ENST00000323829.9:c.*2716-32_*2716-31delinsTA	ENSP00000313025.5:n.*2716-32_*2716-31delinsTA
ENST00000504517.5:c.2858-32_2858-31delinsTA	ENSP00000421779.1:n.2858-32_2858-31delinsTA
ENST00000504690.5:c.3328-32_3328-31delinsTA	ENSP00000425627.1:n.3328-32_3328-31delinsTA
ENST00000510779.1:c.2378-32_2378-31delinsTA
ENST00000512049.5:c.3307-32_3307-31delinsTA	ENSP00000421860.1:n.3307-32_3307-31delinsTA
ENST00000515425.5:c.3328-32_3328-31delinsTA	ENSP00000423660.1:n.3328-32_3328-31delinsTA
NM_024577.3:c.3328-32_3328-31delinsTA , LRG_269t1:c.3328-32_3328-31delinsTA	NP_078853.2:n.3328-32_3328-31delinsTA
NM_024577.4:c.3328-32_3328-31delinsTA MANE Select	NP_078853.2:n.3328-32_3328-31delinsTA