Canonical Allele Identifier: CA393201598
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781023A>G , CM000677.2:g.66781023A>G GRCh38
NC_000015.9:g.67073361A>G , CM000677.1:g.67073361A>G GRCh37
NC_000015.8:g.64860415A>G NCBI36
NG_012244.1:g.83688A>G
NG_012244.2:g.83688A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.979A>G MANE Select ENSP00000288840.5:p.Lys327Glu
ENST00000288840.9:c.979A>G ENSP00000288840.5:p.Lys327Glu
ENST00000557916.5:c.1111A>G ENSP00000452955.1:n.1111A>G
ENST00000559931.5:c.283A>G ENSP00000453446.1:n.283A>G
NM_005585.4:c.979A>G NP_005576.3:p.Lys327Glu
NR_027654.1:n.2034A>G
XM_011521561.1:c.196A>G XP_011519863.1:p.Lys66Glu
XR_931825.1:n.2378A>G
XM_011521561.2:c.196A>G XP_011519863.1:p.Lys66Glu
NM_005585.5:c.979A>G MANE Select NP_005576.3:p.Lys327Glu
NR_027654.2:n.2134A>G