Canonical Allele Identifier: CA393201549

Gene: SMAD6

Linked Data

• gnomAD v4: 15-66781000-C-A
• MyVariant Identifiers: chr15:g.67073338C>A (hg19) ; chr15:g.66781000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781000C>A , CM000677.2:g.66781000C>A	GRCh38
NC_000015.9:g.67073338C>A , CM000677.1:g.67073338C>A	GRCh37
NC_000015.8:g.64860392C>A	NCBI36
NG_012244.1:g.83665C>A
NG_012244.2:g.83665C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.956C>A MANE Select	ENSP00000288840.5:p.Ala319Asp
ENST00000288840.9:c.956C>A	ENSP00000288840.5:p.Ala319Asp
ENST00000557916.5:c.1088C>A	ENSP00000452955.1:n.1088C>A
ENST00000559931.5:c.260C>A	ENSP00000453446.1:n.260C>A
NM_005585.4:c.956C>A	NP_005576.3:p.Ala319Asp
NR_027654.1:n.2011C>A
XM_011521561.1:c.173C>A	XP_011519863.1:p.Ala58Asp
XR_931825.1:n.2355C>A
XM_011521561.2:c.173C>A	XP_011519863.1:p.Ala58Asp
NM_005585.5:c.956C>A MANE Select	NP_005576.3:p.Ala319Asp
NR_027654.2:n.2111C>A