Canonical Allele Identifier: CA9015697

Gene: SHC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.438725G>A , CM000681.2:g.438725G>A	GRCh38
NC_000019.9:g.438725G>A , CM000681.1:g.438725G>A	GRCh37
NC_000019.8:g.389725G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264554.11:c.713C>T MANE Select	ENSP00000264554.4:p.Thr238Met
ENST00000264554.10:c.713C>T	ENSP00000264554.4:p.Thr238Met
ENST00000590113.4:n.209C>T
ENST00000590222.5:c.547C>T
NM_012435.2:c.713C>T	NP_036567.2:p.Thr238Met
XM_011527893.1:c.713C>T	XP_011526195.1:p.Thr238Met
XM_011527894.1:c.713C>T	XP_011526196.1:p.Thr238Met
XM_011527895.1:c.713C>T	XP_011526197.1:p.Thr238Met
XM_011527896.1:c.242C>T	XP_011526198.1:p.Thr81Met
XM_011527893.3:c.713C>T	XP_011526195.1:p.Thr238Met
XM_011527894.2:c.713C>T	XP_011526196.1:p.Thr238Met
XM_011527895.2:c.713C>T	XP_011526197.1:p.Thr238Met
XM_011527896.2:c.242C>T	XP_011526198.1:p.Thr81Met
NM_001387056.1:c.713C>T	NP_001373985.1:p.Thr238Met
NM_012435.3:c.713C>T MANE Select	NP_036567.2:p.Thr238Met