Canonical Allele Identifier: CA402859442

Gene: SHC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.460644T>A , CM000681.2:g.460644T>A	GRCh38
NC_000019.9:g.460644T>A , CM000681.1:g.460644T>A	GRCh37
NC_000019.8:g.411644T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264554.11:c.353A>T MANE Select	ENSP00000264554.4:p.Asp118Val
ENST00000264554.10:c.353A>T	ENSP00000264554.4:p.Asp118Val
NM_012435.2:c.353A>T	NP_036567.2:p.Asp118Val
XM_011527893.1:c.353A>T	XP_011526195.1:p.Asp118Val
XM_011527894.1:c.353A>T	XP_011526196.1:p.Asp118Val
XM_011527895.1:c.353A>T	XP_011526197.1:p.Asp118Val
XM_011527893.3:c.353A>T	XP_011526195.1:p.Asp118Val
XM_011527894.2:c.353A>T	XP_011526196.1:p.Asp118Val
XM_011527895.2:c.353A>T	XP_011526197.1:p.Asp118Val
NM_001387056.1:c.353A>T	NP_001373985.1:p.Asp118Val
NM_012435.3:c.353A>T MANE Select	NP_036567.2:p.Asp118Val