Canonical Allele Identifier: CA2641839547

Gene: SMAD4

Linked Data

• gnomAD v4: 18-51078660-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078660T>C , CM000680.2:g.51078660T>C	GRCh38
NC_000018.9:g.48605030T>C , CM000680.1:g.48605030T>C	GRCh37
NC_000018.8:g.46859028T>C	NCBI36
NG_013013.2:g.115621T>C , LRG_318:g.115621T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*193T>C	ENSP00000465878.2:n.*193T>C
ENST00000589076.6:c.*193T>C	ENSP00000466934.2:n.*193T>C
ENST00000589941.2:c.*193T>C	ENSP00000465874.2:n.*193T>C
ENST00000590061.2:c.*193T>C	ENSP00000464772.2:n.*193T>C
ENST00000593223.2:c.*1849T>C	ENSP00000466118.2:n.*1849T>C
ENST00000611848.2:c.*504T>C	ENSP00000478613.2:n.*504T>C
ENST00000684953.1:n.3867T>C
ENST00000685090.1:n.3782T>C
ENST00000685232.1:n.2073T>C
ENST00000688574.1:n.1960T>C
ENST00000691124.1:n.4813T>C
ENST00000342988.8:c.*193T>C MANE Select	ENSP00000341551.3:n.*193T>C
ENST00000342988.7:c.*193T>C	ENSP00000341551.3:n.*193T>C
ENST00000398417.6:c.*193T>C	ENSP00000381452.1:n.*193T>C
ENST00000586253.1:n.574T>C
ENST00000591126.5:n.3853T>C
ENST00000611848.1:c.1165T>C
NM_005359.5:c.*193T>C , LRG_318t1:c.*193T>C	NP_005350.1:n.*193T>C
NM_005359.6:c.*193T>C MANE Select	NP_005350.1:n.*193T>C