Canonical Allele Identifier: CA878103

Gene: MYSM1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58690418C>T , CM000663.2:g.58690418C>T	GRCh38
NC_000001.10:g.59156090C>T , CM000663.1:g.59156090C>T	GRCh37
NC_000001.9:g.58928678C>T	NCBI36
NG_065323.1:g.14674G>A
NG_065323.2:g.14660G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001085487.3:c.219-1G>A MANE Select	NP_001078956.1:n.219-1G>A
ENST00000472487.6:c.219-1G>A MANE Select	ENSP00000418734.1:n.219-1G>A
NM_001085487.2:c.219-1G>A	NP_001078956.1:n.219-1G>A
ENST00000466774.5:n.247-1G>A
ENST00000472487.5:c.219-1G>A	ENSP00000418734.1:n.219-1G>A
ENST00000483003.5:n.239-1G>A
ENST00000483003.6:n.239-1G>A
ENST00000655340.1:c.219-1G>A	ENSP00000499373.1:n.219-1G>A
ENST00000659108.1:c.219-1G>A	ENSP00000499571.1:n.219-1G>A
ENST00000659812.1:c.166-1G>A
ENST00000659812.2:c.219-1G>A	ENSP00000499686.2:n.219-1G>A
ENST00000660611.1:n.94-1G>A
ENST00000665648.1:c.219-1G>A	ENSP00000499586.1:n.219-1G>A
ENST00000697253.1:c.219-1G>A	ENSP00000513210.1:n.219-1G>A
ENST00000697254.1:c.219-1G>A	ENSP00000513211.1:n.219-1G>A
ENST00000697255.1:c.219-1G>A	ENSP00000513212.1:n.219-1G>A
ENST00000697257.1:n.229-1G>A
ENST00000697261.1:n.235-1G>A
ENST00000697263.1:n.239-1G>A
XM_006710314.2:c.219-1G>A	XP_006710377.1:n.219-1G>A
XM_006710314.3:c.219-1G>A	XP_006710377.1:n.219-1G>A
XM_011540573.1:c.18-1G>A	XP_011538875.1:n.18-1G>A
XM_011540573.3:c.18-1G>A	XP_011538875.1:n.18-1G>A
XM_011540574.2:c.-300-1G>A	XP_011538876.1:n.-300-1G>A
XR_246231.3:n.259-1G>A
XR_246231.4:n.258-1G>A
XR_946533.1:n.259-1G>A
XR_946533.2:n.258-1G>A