Canonical Allele Identifier: CA2740941792

Gene: CHCHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.56212803A>T , CM000670.2:g.56212803A>T	GRCh38
NC_000008.10:g.57125362A>T , CM000670.1:g.57125362A>T	GRCh37
NC_000008.9:g.57287916A>T	NCBI36
NG_023310.1:g.3498T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355315.8:c.-17+966A>T MANE Select	ENSP00000347469.3:n.-17+966A>T
ENST00000303759.3:c.-48A>T	ENSP00000306425.3:n.-48A>T
ENST00000355315.7:c.-17+966A>T	ENSP00000347469.3:n.-17+966A>T
ENST00000396723.9:c.-96A>T	ENSP00000379949.5:n.-96A>T
ENST00000517636.5:c.-17+629A>T	ENSP00000429230.1:n.-17+629A>T
ENST00000517933.5:c.-17+966A>T	ENSP00000430350.1:n.-17+966A>T
ENST00000518169.1:n.94A>T
ENST00000518801.5:c.-67A>T	ENSP00000428274.1:n.-67A>T
ENST00000521524.5:c.-67A>T	ENSP00000430458.1:n.-67A>T
ENST00000521831.5:c.-17+966A>T	ENSP00000429635.1:n.-17+966A>T
ENST00000521982.5:c.-96A>T	ENSP00000430714.1:n.-96A>T
ENST00000522166.1:n.1015A>T
ENST00000522366.5:n.49+966A>T
ENST00000523061.5:c.-17+966A>T	ENSP00000430882.1:n.-17+966A>T
ENST00000523532.5:c.-96A>T	ENSP00000430498.1:n.-96A>T
ENST00000523667.5:c.-96A>T	ENSP00000429217.1:n.-96A>T
ENST00000523975.5:c.-67A>T	ENSP00000428917.1:n.-67A>T
NM_001011667.1:c.-48A>T	NP_001011667.1:n.-48A>T
NM_001011668.1:c.-48A>T	NP_001011668.1:n.-48A>T
NM_001011669.1:c.-67A>T	NP_001011669.1:n.-67A>T
NM_001011670.1:c.-17+966A>T	NP_001011670.1:n.-17+966A>T
NM_001011671.1:c.-17+966A>T	NP_001011671.1:n.-17+966A>T
NM_024300.3:c.-67A>T	NP_077276.2:n.-67A>T
XR_428340.1:n.91A>T
NM_001011667.2:c.-48A>T	NP_001011667.1:n.-48A>T
NM_001011668.2:c.-48A>T	NP_001011668.1:n.-48A>T
NM_001011669.2:c.-67A>T	NP_001011669.1:n.-67A>T
NM_001011670.2:c.-17+966A>T	NP_001011670.1:n.-17+966A>T
NM_001011671.2:c.-17+966A>T	NP_001011671.1:n.-17+966A>T
NM_001317858.1:c.-67A>T	NP_001304787.1:n.-67A>T
NM_001317859.1:c.-17+966A>T	NP_001304788.1:n.-17+966A>T
NM_024300.4:c.-67A>T	NP_077276.2:n.-67A>T
NR_133934.1:n.242A>T
NR_133935.1:n.242A>T
NR_133936.1:n.242A>T
NR_133937.1:n.200+966A>T
NM_001011671.3:c.-17+966A>T MANE Select	NP_001011671.1:n.-17+966A>T
NM_001011667.3:c.-48A>T	NP_001011667.1:n.-48A>T
NM_001011668.3:c.-48A>T	NP_001011668.1:n.-48A>T
NM_001011669.3:c.-67A>T	NP_001011669.1:n.-67A>T
NM_001011670.3:c.-17+966A>T	NP_001011670.1:n.-17+966A>T
NM_001317858.2:c.-67A>T	NP_001304787.1:n.-67A>T
NM_001317859.2:c.-17+966A>T	NP_001304788.1:n.-17+966A>T
NM_024300.5:c.-67A>T	NP_077276.2:n.-67A>T
NR_133934.2:n.91A>T
NR_133935.2:n.91A>T
NR_133936.2:n.91A>T
NR_133937.2:n.49+966A>T