Canonical Allele Identifier: CA393201679

Gene: SMAD6

Linked Data

• MyVariant Identifiers: chr15:g.67073395A>T (hg19) ; chr15:g.66781057A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781057A>T , CM000677.2:g.66781057A>T	GRCh38
NC_000015.9:g.67073395A>T , CM000677.1:g.67073395A>T	GRCh37
NC_000015.8:g.64860449A>T	NCBI36
NG_012244.1:g.83722A>T
NG_012244.2:g.83722A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.1013A>T MANE Select	ENSP00000288840.5:p.Glu338Val
ENST00000288840.9:c.1013A>T	ENSP00000288840.5:p.Glu338Val
ENST00000557916.5:c.1145A>T	ENSP00000452955.1:n.1145A>T
ENST00000559931.5:c.317A>T	ENSP00000453446.1:n.317A>T
NM_005585.4:c.1013A>T	NP_005576.3:p.Glu338Val
NR_027654.1:n.2068A>T
XM_011521561.1:c.230A>T	XP_011519863.1:p.Glu77Val
XR_931825.1:n.2412A>T
XM_011521561.2:c.230A>T	XP_011519863.1:p.Glu77Val
NM_005585.5:c.1013A>T MANE Select	NP_005576.3:p.Glu338Val
NR_027654.2:n.2168A>T