Canonical Allele Identifier: CA1912982817

Gene: TFAM

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.58385582G= , CM000672.2:g.58385582G=	GRCh38
NC_000010.10:g.60145342G= , CM000672.1:g.60145342G=	GRCh37
NC_000010.9:g.59815348G=	NCBI36
NG_053006.1:g.5440G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487519.6:c.35G= MANE Select	ENSP00000420588.1:p.Ser12=
ENST00000373895.7:c.35G=	ENSP00000363002.3:p.Ser12=
ENST00000373899.3:n.238G=
ENST00000487519.5:c.35G=	ENSP00000420588.1:p.Ser12=
NM_001270782.1:c.35G=	NP_001257711.1:p.Ser12=
NM_003201.2:c.35G=	NP_003192.1:p.Ser12=
NR_073073.1:n.440G=
XM_011540120.1:c.35G=	XP_011538422.1:p.Ser12=
XM_011540121.1:c.35G=	XP_011538423.1:p.Ser12=
XM_011540121.3:c.35G=	XP_011538423.1:p.Ser12=
NM_003201.3:c.35G= MANE Select	NP_003192.1:p.Ser12=
NM_001270782.2:c.35G=	NP_001257711.1:p.Ser12=
NR_073073.2:n.173G=