Canonical Allele Identifier: CA629587075

Gene: SMAD4

Linked Data

• gnomAD v2: 18-48575596-T-C
• gnomAD v4: 18-51049226-T-C
• MyVariant Identifiers: chr18:g.48575596T>C (hg19) ; chr18:g.51049226T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51049226T>C , CM000680.2:g.51049226T>C	GRCh38
NC_000018.9:g.48575596T>C , CM000680.1:g.48575596T>C	GRCh37
NC_000018.8:g.46829594T>C	NCBI36
NG_013013.2:g.86187T>C , LRG_318:g.86187T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.425-69T>C	ENSP00000465878.2:n.425-69T>C
ENST00000589076.6:c.425-69T>C	ENSP00000466934.2:n.425-69T>C
ENST00000589941.2:c.425-69T>C	ENSP00000465874.2:n.425-69T>C
ENST00000590061.2:c.425-69T>C	ENSP00000464772.2:n.425-69T>C
ENST00000593223.2:c.425-69T>C	ENSP00000466118.2:n.425-69T>C
ENST00000611848.2:c.425-69T>C	ENSP00000478613.2:n.425-69T>C
ENST00000342988.8:c.425-69T>C MANE Select	ENSP00000341551.3:n.425-69T>C
ENST00000342988.7:c.425-69T>C	ENSP00000341551.3:n.425-69T>C
ENST00000398417.6:c.425-69T>C	ENSP00000381452.1:n.425-69T>C
ENST00000588745.5:c.425-69T>C	ENSP00000464901.1:n.425-69T>C
ENST00000589706.1:n.293-69T>C
ENST00000590722.2:c.*448-69T>C	ENSP00000465737.1:n.*448-69T>C
ENST00000591914.5:c.425-69T>C	ENSP00000466941.1:n.425-69T>C
ENST00000592186.5:c.425-69T>C	ENSP00000468611.1:n.425-69T>C
ENST00000592911.5:n.203-69T>C
NM_005359.5:c.425-69T>C , LRG_318t1:c.425-69T>C	NP_005350.1:n.425-69T>C
NM_005359.6:c.425-69T>C MANE Select	NP_005350.1:n.425-69T>C