Canonical Allele Identifier: CA393201775
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781104G>C , CM000677.2:g.66781104G>C GRCh38
NC_000015.9:g.67073442G>C , CM000677.1:g.67073442G>C GRCh37
NC_000015.8:g.64860496G>C NCBI36
NG_012244.1:g.83769G>C
NG_012244.2:g.83769G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1060G>C MANE Select ENSP00000288840.5:p.Val354Leu
ENST00000288840.9:c.1060G>C ENSP00000288840.5:p.Val354Leu
ENST00000557916.5:c.1192G>C ENSP00000452955.1:n.1192G>C
ENST00000559931.5:c.364G>C ENSP00000453446.1:n.364G>C
NM_005585.4:c.1060G>C NP_005576.3:p.Val354Leu
NR_027654.1:n.2115G>C
XM_011521561.1:c.277G>C XP_011519863.1:p.Val93Leu
XR_931825.1:n.2459G>C
XM_011521561.2:c.277G>C XP_011519863.1:p.Val93Leu
NM_005585.5:c.1060G>C MANE Select NP_005576.3:p.Val354Leu
NR_027654.2:n.2215G>C