Canonical Allele Identifier: CA393201798

Gene: SMAD6

Linked Data

• MyVariant Identifiers: chr15:g.67073452T>A (hg19) ; chr15:g.66781114T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781114T>A , CM000677.2:g.66781114T>A	GRCh38
NC_000015.9:g.67073452T>A , CM000677.1:g.67073452T>A	GRCh37
NC_000015.8:g.64860506T>A	NCBI36
NG_012244.1:g.83779T>A
NG_012244.2:g.83779T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.1070T>A MANE Select	ENSP00000288840.5:p.Phe357Tyr
ENST00000288840.9:c.1070T>A	ENSP00000288840.5:p.Phe357Tyr
ENST00000557916.5:c.1202T>A	ENSP00000452955.1:n.1202T>A
ENST00000559931.5:c.374T>A	ENSP00000453446.1:n.374T>A
NM_005585.4:c.1070T>A	NP_005576.3:p.Phe357Tyr
NR_027654.1:n.2125T>A
XM_011521561.1:c.287T>A	XP_011519863.1:p.Phe96Tyr
XR_931825.1:n.2469T>A
XM_011521561.2:c.287T>A	XP_011519863.1:p.Phe96Tyr
NM_005585.5:c.1070T>A MANE Select	NP_005576.3:p.Phe357Tyr
NR_027654.2:n.2225T>A