Canonical Allele Identifier: CA393201557
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781004C>A , CM000677.2:g.66781004C>A GRCh38
NC_000015.9:g.67073342C>A , CM000677.1:g.67073342C>A GRCh37
NC_000015.8:g.64860396C>A NCBI36
NG_012244.1:g.83669C>A
NG_012244.2:g.83669C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.960C>A MANE Select ENSP00000288840.5:p.Ser320Arg
ENST00000288840.9:c.960C>A ENSP00000288840.5:p.Ser320Arg
ENST00000557916.5:c.1092C>A ENSP00000452955.1:n.1092C>A
ENST00000559931.5:c.264C>A ENSP00000453446.1:n.264C>A
NM_005585.4:c.960C>A NP_005576.3:p.Ser320Arg
NR_027654.1:n.2015C>A
XM_011521561.1:c.177C>A XP_011519863.1:p.Ser59Arg
XR_931825.1:n.2359C>A
XM_011521561.2:c.177C>A XP_011519863.1:p.Ser59Arg
NM_005585.5:c.960C>A MANE Select NP_005576.3:p.Ser320Arg
NR_027654.2:n.2115C>A