Canonical Allele Identifier: CA372433862

Gene: MROH6

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143569575C>A , CM000670.2:g.143569575C>A	GRCh38
NC_000008.10:g.144651745C>A , CM000670.1:g.144651745C>A	GRCh37
NC_000008.9:g.144722888C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001100878.2:c.1342G>T MANE Select	NP_001094348.1:p.Ala448Ser
ENST00000398882.8:c.1342G>T MANE Select	ENSP00000381857.3:p.Ala448Ser
NM_001100878.1:c.1342G>T	NP_001094348.1:p.Ala448Ser
ENST00000398882.7:c.1342G>T	ENSP00000381857.3:p.Ala448Ser
ENST00000529971.1:c.1379G>T	ENSP00000436959.1:p.Arg460Leu
ENST00000533679.5:c.-546G>T	ENSP00000434244.1:n.-546G>T
XM_006716615.2:c.1345G>T	XP_006716678.1:p.Ala449Ser
XM_011517214.1:c.1345G>T	XP_011515516.1:p.Ala449Ser
XM_011517215.1:c.1342G>T	XP_011515517.1:p.Ala448Ser
XM_011517216.1:c.1345G>T	XP_011515518.1:p.Ala449Ser
XM_011517216.2:c.1345G>T	XP_011515518.1:p.Ala449Ser
XM_011517217.1:c.1345G>T	XP_011515519.1:p.Ala449Ser
XM_011517218.1:c.1345G>T	XP_011515520.1:p.Ala449Ser
XM_011517219.1:c.1345G>T	XP_011515521.1:p.Ala449Ser
XM_011517220.1:c.1345G>T	XP_011515522.1:p.Ala449Ser
XM_011517221.1:c.1345G>T	XP_011515523.1:p.Ala449Ser
XM_011517221.2:c.1345G>T	XP_011515523.1:p.Ala449Ser
XM_011517222.1:c.1345G>T	XP_011515524.1:p.Ala449Ser
XM_011517223.1:c.1345G>T	XP_011515525.1:p.Ala449Ser
XM_011517224.1:c.1232G>T	XP_011515526.1:p.Arg411Leu
XR_928344.1:n.1270G>T
XR_928345.1:n.1270G>T
XR_928346.1:n.1267G>T