Canonical Allele Identifier: CA352728320

Gene: NDUFAF3

Linked Data

• MyVariant Identifiers: chr3:g.49059916G>T (hg19) ; chr3:g.49022483G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49022483G>T , CM000665.2:g.49022483G>T	GRCh38
NC_000003.11:g.49059916G>T , CM000665.1:g.49059916G>T	GRCh37
NC_000003.10:g.49034920G>T	NCBI36
NG_012091.1:g.11960C>A
NG_016282.1:g.7009G>T
NG_033126.1:g.3589C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326925.11:c.215G>T MANE Select	ENSP00000323076.5:p.Gly72Val
ENST00000326912.8:c.44G>T	ENSP00000323003.4:p.Gly15Val
ENST00000326925.10:c.215G>T	ENSP00000323076.5:p.Gly72Val
ENST00000395458.6:c.44G>T	ENSP00000378843.2:p.Gly15Val
ENST00000451378.2:c.44G>T	ENSP00000402465.2:p.Gly15Val
ENST00000480392.1:n.239G>T
ENST00000496152.1:n.371G>T
NM_199069.1:c.215G>T	NP_951032.1:p.Gly72Val
NM_199070.1:c.44G>T	NP_951033.1:p.Gly15Val
NM_199073.1:c.44G>T	NP_951047.1:p.Gly15Val
NM_199074.1:c.44G>T	NP_951056.1:p.Gly15Val
NM_199069.2:c.215G>T MANE Select	NP_951032.1:p.Gly72Val
NM_199070.2:c.44G>T	NP_951033.1:p.Gly15Val
NM_199073.2:c.44G>T	NP_951047.1:p.Gly15Val
NM_199074.2:c.44G>T	NP_951056.1:p.Gly15Val