Canonical Allele Identifier: CA393201795
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781113T>G , CM000677.2:g.66781113T>G GRCh38
NC_000015.9:g.67073451T>G , CM000677.1:g.67073451T>G GRCh37
NC_000015.8:g.64860505T>G NCBI36
NG_012244.1:g.83778T>G
NG_012244.2:g.83778T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005585.5:c.1069T>G MANE Select NP_005576.3:p.Phe357Val
ENST00000288840.10:c.1069T>G MANE Select ENSP00000288840.5:p.Phe357Val
NM_005585.4:c.1069T>G NP_005576.3:p.Phe357Val
NR_027654.1:n.2124T>G
NR_027654.2:n.2224T>G
ENST00000288840.9:c.1069T>G ENSP00000288840.5:p.Phe357Val
ENST00000557916.5:c.1201T>G ENSP00000452955.1:n.1201T>G
ENST00000559931.5:c.373T>G ENSP00000453446.1:n.373T>G
XM_011521561.1:c.286T>G XP_011519863.1:p.Phe96Val
XM_011521561.2:c.286T>G XP_011519863.1:p.Phe96Val
XR_931825.1:n.2468T>G