Canonical Allele Identifier: CA2184231433
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs1894423684

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66774028_66774029insG , CM000677.2:g.66774028_66774029insG GRCh38
NC_000015.9:g.67066366_67066367insG , CM000677.1:g.67066366_67066367insG GRCh37
NC_000015.8:g.64853420_64853421insG NCBI36
NG_012244.1:g.76693_76694insG
NG_012244.2:g.76693_76694insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.953-6969_953-6968insG MANE Select ENSP00000288840.5:n.953-6969_953-6968insG
ENST00000288840.9:c.953-6969_953-6968insG ENSP00000288840.5:n.953-6969_953-6968insG
ENST00000557916.5:c.1085-6969_1085-6968insG ENSP00000452955.1:n.1085-6969_1085-6968insG
ENST00000559931.5:c.257-6969_257-6968insG ENSP00000453446.1:n.257-6969_257-6968insG
NM_005585.4:c.953-6969_953-6968insG NP_005576.3:n.953-6969_953-6968insG
NR_027654.1:n.2008-6969_2008-6968insG
XM_011521561.1:c.170-6969_170-6968insG XP_011519863.1:n.170-6969_170-6968insG
XR_931825.1:n.2352-6969_2352-6968insG
XM_011521561.2:c.170-6969_170-6968insG XP_011519863.1:n.170-6969_170-6968insG
NM_005585.5:c.953-6969_953-6968insG MANE Select NP_005576.3:n.953-6969_953-6968insG
NR_027654.2:n.2108-6969_2108-6968insG