Canonical Allele Identifier: CA402465075

Gene: SMAD4

Linked Data

• gnomAD v4: 18-51067183-T-C
• MyVariant Identifiers: chr18:g.48593553T>C (hg19) ; chr18:g.51067183T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51067183T>C , CM000680.2:g.51067183T>C	GRCh38
NC_000018.9:g.48593553T>C , CM000680.1:g.48593553T>C	GRCh37
NC_000018.8:g.46847551T>C	NCBI36
NG_013013.2:g.104144T>C , LRG_318:g.104144T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1304T>C	ENSP00000465878.2:p.Ile435Thr
ENST00000589076.6:c.1304T>C	ENSP00000466934.2:p.Ile435Thr
ENST00000589941.2:c.1304T>C	ENSP00000465874.2:p.Ile435Thr
ENST00000590061.2:c.1304T>C	ENSP00000464772.2:p.Ile435Thr
ENST00000593223.2:c.1304T>C	ENSP00000466118.2:p.Ile435Thr
ENST00000611848.2:c.1304T>C	ENSP00000478613.2:p.Ile435Thr
ENST00000684953.1:n.2676T>C
ENST00000685090.1:n.1755T>C
ENST00000685232.1:n.1412T>C
ENST00000688574.1:n.1412T>C
ENST00000691124.1:n.2786T>C
ENST00000342988.8:c.1304T>C MANE Select	ENSP00000341551.3:p.Ile435Thr
ENST00000342988.7:c.1304T>C	ENSP00000341551.3:p.Ile435Thr
ENST00000398417.6:c.1304T>C	ENSP00000381452.1:p.Ile435Thr
ENST00000588745.5:c.1016T>C	ENSP00000464901.1:p.Ile339Thr
ENST00000590499.1:n.362T>C
ENST00000591126.5:n.3305T>C
ENST00000592186.5:c.955+7267T>C	ENSP00000468611.1:n.955+7267T>C
ENST00000593223.1:c.71T>C	ENSP00000466118.1:p.Ile24Thr
ENST00000611848.1:c.504T>C
NM_005359.5:c.1304T>C , LRG_318t1:c.1304T>C	NP_005350.1:p.Ile435Thr
NM_005359.6:c.1304T>C MANE Select	NP_005350.1:p.Ile435Thr