Canonical Allele Identifier: CA13381822
Gene: MTCH2 HGNC NCBI

Linked Data

dbSNP Id: rs4752856

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47626490G>A , CM000673.2:g.47626490G>A GRCh38
NC_000011.9:g.47648042G>A , CM000673.1:g.47648042G>A GRCh37
NC_000011.8:g.47604618G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530428.2:c.654+590C>T ENSP00000432043.2:n.654+590C>T
ENST00000533571.2:n.728+590C>T
ENST00000302503.8:c.681+590C>T MANE Select ENSP00000303222.3:n.681+590C>T
ENST00000302503.7:c.681+590C>T ENSP00000303222.3:n.681+590C>T
ENST00000525649.5:n.374+590C>T
ENST00000530428.1:c.654+590C>T ENSP00000432043.1:n.654+590C>T
ENST00000534074.5:n.451+590C>T
ENST00000539759.5:n.356+8182C>T
NM_014342.3:c.681+590C>T NP_055157.1:n.681+590C>T
XM_006718172.2:c.681+590C>T XP_006718235.1:n.681+590C>T
XM_011519959.1:c.681+590C>T XP_011518261.1:n.681+590C>T
XM_011519960.1:c.654+590C>T XP_011518262.1:n.654+590C>T
XM_011519961.1:c.681+590C>T XP_011518263.1:n.681+590C>T
XM_011519963.1:c.300+590C>T XP_011518265.1:n.300+590C>T
NM_001317231.1:c.681+590C>T NP_001304160.1:n.681+590C>T
NM_001317232.1:c.654+590C>T NP_001304161.1:n.654+590C>T
NM_001317233.1:c.237+590C>T NP_001304162.1:n.237+590C>T
XM_011519959.2:c.681+590C>T XP_011518261.1:n.681+590C>T
XM_011519960.3:c.654+590C>T XP_011518262.1:n.654+590C>T
XM_011519961.2:c.681+590C>T XP_011518263.1:n.681+590C>T
XM_017017462.2:c.654+590C>T XP_016872951.1:n.654+590C>T
NM_014342.4:c.681+590C>T MANE Select NP_055157.1:n.681+590C>T
NM_001317231.2:c.681+590C>T NP_001304160.1:n.681+590C>T
NM_001317232.2:c.654+590C>T NP_001304161.1:n.654+590C>T
NM_001317233.2:c.237+590C>T NP_001304162.1:n.237+590C>T