Canonical Allele Identifier: CA1590317328

Gene: SH3TC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149038388G= , CM000667.2:g.149038388G=	GRCh38
NC_000005.9:g.148417951G= , CM000667.1:g.148417951G=	GRCh37
NC_000005.8:g.148398144G=	NCBI36
NG_007947.2:g.29787C= , LRG_269:g.29787C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000502274.2:c.798C=
ENST00000515425.6:c.908C= MANE Select	ENSP00000423660.1:p.Pro303=
ENST00000674655.1:c.170C=	ENSP00000502840.1:p.Pro57=
ENST00000674983.1:c.*166C=	ENSP00000502387.1:n.*166C=
ENST00000675793.1:c.908C=	ENSP00000502039.1:p.Pro303=
ENST00000676056.1:c.*166C=	ENSP00000501827.1:n.*166C=
ENST00000323829.9:c.*166C=	ENSP00000313025.5:n.*166C=
ENST00000503071.1:n.375C=
ENST00000504517.5:c.308C=	ENSP00000421779.1:p.Pro103=
ENST00000504690.5:c.908C=	ENSP00000425627.1:p.Pro303=
ENST00000511307.5:c.*688C=	ENSP00000421420.1:n.*688C=
ENST00000512049.5:c.887C=	ENSP00000421860.1:p.Pro296=
ENST00000513604.5:c.*166C=	ENSP00000423111.1:n.*166C=
ENST00000515425.5:c.908C=	ENSP00000423660.1:p.Pro303=
NM_024577.3:c.908C= , LRG_269t1:c.908C=	NP_078853.2:p.Pro303=
NM_024577.4:c.908C= MANE Select	NP_078853.2:p.Pro303=