Canonical Allele Identifier: CA1969482632

Gene: MTCH2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47641423A= , CM000673.2:g.47641423A=	GRCh38
NC_000011.9:g.47662975A= , CM000673.1:g.47662975A=	GRCh37
NC_000011.8:g.47619551A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000530428.2:c.87+956T=	ENSP00000432043.2:n.87+956T=
ENST00000533571.2:n.134+978T=
ENST00000302503.8:c.87+956T= MANE Select	ENSP00000303222.3:n.87+956T=
ENST00000302503.7:c.87+956T=	ENSP00000303222.3:n.87+956T=
ENST00000530428.1:c.87+956T=	ENSP00000432043.1:n.87+956T=
ENST00000533571.1:n.195+978T=
ENST00000539759.5:n.74+956T=
NM_014342.3:c.87+956T=	NP_055157.1:n.87+956T=
XM_006718172.2:c.87+956T=	XP_006718235.1:n.87+956T=
XM_011519959.1:c.87+956T=	XP_011518261.1:n.87+956T=
XM_011519960.1:c.87+956T=	XP_011518262.1:n.87+956T=
XM_011519961.1:c.87+956T=	XP_011518263.1:n.87+956T=
XM_011519962.1:c.87+956T=	XP_011518264.1:n.87+956T=
XM_011519963.1:c.-295+978T=	XP_011518265.1:n.-295+978T=
NM_001317231.1:c.87+956T=	NP_001304160.1:n.87+956T=
NM_001317232.1:c.87+956T=	NP_001304161.1:n.87+956T=
NM_001317233.1:c.-300+956T=	NP_001304162.1:n.-300+956T=
XM_011519959.2:c.87+956T=	XP_011518261.1:n.87+956T=
XM_011519960.3:c.87+956T=	XP_011518262.1:n.87+956T=
XM_011519961.2:c.87+956T=	XP_011518263.1:n.87+956T=
XM_017017462.2:c.87+956T=	XP_016872951.1:n.87+956T=
NM_014342.4:c.87+956T= MANE Select	NP_055157.1:n.87+956T=
NM_001317231.2:c.87+956T=	NP_001304160.1:n.87+956T=
NM_001317232.2:c.87+956T=	NP_001304161.1:n.87+956T=
NM_001317233.2:c.-300+956T=	NP_001304162.1:n.-300+956T=