Canonical Allele Identifier: CA593906930

Gene: TFAM

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.58388932A>C , CM000672.2:g.58388932A>C	GRCh38
NC_000010.10:g.60148692A>C , CM000672.1:g.60148692A>C	GRCh37
NC_000010.9:g.59818698A>C	NCBI36
NG_053006.1:g.8790A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487519.6:c.441+113A>C MANE Select	ENSP00000420588.1:n.441+113A>C
ENST00000373895.7:c.441+113A>C	ENSP00000363002.3:n.441+113A>C
ENST00000373899.3:n.711+113A>C
ENST00000395377.2:c.385+113A>C
ENST00000487519.5:c.441+113A>C	ENSP00000420588.1:n.441+113A>C
NM_001270782.1:c.441+113A>C	NP_001257711.1:n.441+113A>C
NM_003201.2:c.441+113A>C	NP_003192.1:n.441+113A>C
NR_073073.1:n.913+113A>C
XM_011540120.1:c.442-20A>C	XP_011538422.1:n.442-20A>C
XM_011540121.1:c.440+114A>C	XP_011538423.1:n.440+114A>C
XM_011540121.3:c.440+114A>C	XP_011538423.1:n.440+114A>C
NM_003201.3:c.441+113A>C MANE Select	NP_003192.1:n.441+113A>C
NM_001270782.2:c.441+113A>C	NP_001257711.1:n.441+113A>C
NR_073073.2:n.646+113A>C