Canonical Allele Identifier: CA2184234692
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781097C= , CM000677.2:g.66781097C= GRCh38
NC_000015.9:g.67073435C= , CM000677.1:g.67073435C= GRCh37
NC_000015.8:g.64860489C= NCBI36
NG_012244.1:g.83762C=
NG_012244.2:g.83762C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1053C= MANE Select ENSP00000288840.5:p.Asp351=
ENST00000288840.9:c.1053C= ENSP00000288840.5:p.Asp351=
ENST00000557916.5:c.1185C= ENSP00000452955.1:n.1185C=
ENST00000559931.5:c.357C= ENSP00000453446.1:n.357C=
NM_005585.4:c.1053C= NP_005576.3:p.Asp351=
NR_027654.1:n.2108C=
XM_011521561.1:c.270C= XP_011519863.1:p.Asp90=
XR_931825.1:n.2452C=
XM_011521561.2:c.270C= XP_011519863.1:p.Asp90=
NM_005585.5:c.1053C= MANE Select NP_005576.3:p.Asp351=
NR_027654.2:n.2208C=