Canonical Allele Identifier: CA393201803

Gene: SMAD6

Linked Data

• MyVariant Identifiers: chr15:g.67073455A>T (hg19) ; chr15:g.66781117A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.66781117A>T , CM000677.2:g.66781117A>T	GRCh38
NC_000015.9:g.67073455A>T , CM000677.1:g.67073455A>T	GRCh37
NC_000015.8:g.64860509A>T	NCBI36
NG_012244.1:g.83782A>T
NG_012244.2:g.83782A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288840.10:c.1073A>T MANE Select	ENSP00000288840.5:p.Tyr358Phe
ENST00000288840.9:c.1073A>T	ENSP00000288840.5:p.Tyr358Phe
ENST00000557916.5:c.1205A>T	ENSP00000452955.1:n.1205A>T
ENST00000559931.5:c.377A>T	ENSP00000453446.1:n.377A>T
NM_005585.4:c.1073A>T	NP_005576.3:p.Tyr358Phe
NR_027654.1:n.2128A>T
XM_011521561.1:c.290A>T	XP_011519863.1:p.Tyr97Phe
XR_931825.1:n.2472A>T
XM_011521561.2:c.290A>T	XP_011519863.1:p.Tyr97Phe
NM_005585.5:c.1073A>T MANE Select	NP_005576.3:p.Tyr358Phe
NR_027654.2:n.2228A>T