Canonical Allele Identifier: CA393201562
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781006T>A , CM000677.2:g.66781006T>A GRCh38
NC_000015.9:g.67073344T>A , CM000677.1:g.67073344T>A GRCh37
NC_000015.8:g.64860398T>A NCBI36
NG_012244.1:g.83671T>A
NG_012244.2:g.83671T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.962T>A MANE Select ENSP00000288840.5:p.Met321Lys
ENST00000288840.9:c.962T>A ENSP00000288840.5:p.Met321Lys
ENST00000557916.5:c.1094T>A ENSP00000452955.1:n.1094T>A
ENST00000559931.5:c.266T>A ENSP00000453446.1:n.266T>A
NM_005585.4:c.962T>A NP_005576.3:p.Met321Lys
NR_027654.1:n.2017T>A
XM_011521561.1:c.179T>A XP_011519863.1:p.Met60Lys
XR_931825.1:n.2361T>A
XM_011521561.2:c.179T>A XP_011519863.1:p.Met60Lys
NM_005585.5:c.962T>A MANE Select NP_005576.3:p.Met321Lys
NR_027654.2:n.2117T>A