Canonical Allele Identifier: CA1590304156

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149008717_149008719delinsGTC , CM000667.2:g.149008717_149008719delinsGTC	GRCh38
NC_000005.9:g.148388280_148388282delinsGTC , CM000667.1:g.148388280_148388282delinsGTC	GRCh37
NC_000005.8:g.148368473_148368475delinsGTC	NCBI36
NG_007947.2:g.59456_59458delinsGAC , LRG_269:g.59456_59458delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502274.2:c.3374+132_3374+134delinsGAC
ENST00000515425.6:c.3478+132_3478+134delinsGAC MANE Select	ENSP00000423660.1:n.3478+132_3478+134delinsGAC
ENST00000675793.1:c.*2894_*2896delinsGAC	ENSP00000502039.1:n.*2894_*2896delinsGAC
ENST00000323829.9:c.*2866+132_*2866+134delinsGAC	ENSP00000313025.5:n.*2866+132_*2866+134delinsGAC
ENST00000504517.5:c.3008+132_3008+134delinsGAC	ENSP00000421779.1:n.3008+132_3008+134delinsGAC
ENST00000504690.5:c.3478+132_3478+134delinsGAC	ENSP00000425627.1:n.3478+132_3478+134delinsGAC
ENST00000510779.1:c.2528+132_2528+134delinsGAC
ENST00000512049.5:c.3457+132_3457+134delinsGAC	ENSP00000421860.1:n.3457+132_3457+134delinsGAC
ENST00000515229.5:n.140+132_140+134delinsGAC
ENST00000515425.5:c.3478+132_3478+134delinsGAC	ENSP00000423660.1:n.3478+132_3478+134delinsGAC
NM_024577.3:c.3478+132_3478+134delinsGAC , LRG_269t1:c.3478+132_3478+134delinsGAC	NP_078853.2:n.3478+132_3478+134delinsGAC
NM_024577.4:c.3478+132_3478+134delinsGAC MANE Select	NP_078853.2:n.3478+132_3478+134delinsGAC