Canonical Allele Identifier: CA393201979
Community Standard Title: NM_005585.5(SMAD6):c.1158G>C (p.Lys386Asn)
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781202G>C , CM000677.2:g.66781202G>C GRCh38
NC_000015.9:g.67073540G>C , CM000677.1:g.67073540G>C GRCh37
NC_000015.8:g.64860594G>C NCBI36
NG_012244.1:g.83867G>C
NG_012244.2:g.83867G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005585.5:c.1158G>C MANE Select NP_005576.3:p.Lys386Asn
ENST00000288840.10:c.1158G>C MANE Select ENSP00000288840.5:p.Lys386Asn
NM_005585.4:c.1158G>C NP_005576.3:p.Lys386Asn
NR_027654.1:n.2213G>C
NR_027654.2:n.2313G>C
ENST00000288840.9:c.1158G>C ENSP00000288840.5:p.Lys386Asn
ENST00000557916.5:c.1290G>C ENSP00000452955.1:n.1290G>C
ENST00000559931.5:c.462G>C ENSP00000453446.1:n.462G>C
XM_011521561.1:c.375G>C XP_011519863.1:p.Lys125Asn
XM_011521561.2:c.375G>C XP_011519863.1:p.Lys125Asn
XR_931825.1:n.2557G>C