Canonical Allele Identifier: CA402463425

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 3070255
• ClinVar RCV Id: RCV004011773
• MyVariant Identifiers: chr18:g.48584752C>T (hg19) ; chr18:g.51058382C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51058382C>T , CM000680.2:g.51058382C>T	GRCh38
NC_000018.9:g.48584752C>T , CM000680.1:g.48584752C>T	GRCh37
NC_000018.8:g.46838750C>T	NCBI36
NG_013013.2:g.95343C>T , LRG_318:g.95343C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.830C>T	ENSP00000465878.2:p.Thr277Ile
ENST00000589076.6:c.830C>T	ENSP00000466934.2:p.Thr277Ile
ENST00000589941.2:c.830C>T	ENSP00000465874.2:p.Thr277Ile
ENST00000590061.2:c.830C>T	ENSP00000464772.2:p.Thr277Ile
ENST00000593223.2:c.830C>T	ENSP00000466118.2:p.Thr277Ile
ENST00000611848.2:c.830C>T	ENSP00000478613.2:p.Thr277Ile
ENST00000684953.1:n.2202C>T
ENST00000685232.1:n.938C>T
ENST00000688307.1:n.156-1484C>T
ENST00000688574.1:n.938C>T
ENST00000688903.1:n.1044C>T
ENST00000690892.1:n.938C>T
ENST00000342988.8:c.830C>T MANE Select	ENSP00000341551.3:p.Thr277Ile
ENST00000342988.7:c.830C>T	ENSP00000341551.3:p.Thr277Ile
ENST00000398417.6:c.830C>T	ENSP00000381452.1:p.Thr277Ile
ENST00000588745.5:c.667+3389C>T	ENSP00000464901.1:n.667+3389C>T
ENST00000591126.5:n.2831C>T
ENST00000592186.5:c.830C>T	ENSP00000468611.1:p.Thr277Ile
ENST00000611848.1:c.30C>T
NM_005359.5:c.830C>T , LRG_318t1:c.830C>T	NP_005350.1:p.Thr277Ile
NM_005359.6:c.830C>T MANE Select	NP_005350.1:p.Thr277Ile