Canonical Allele Identifier: CA2496487417

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206145020T= , CM000664.2:g.206145020T=	GRCh38
NC_000002.11:g.207009744T= , CM000664.1:g.207009744T=	GRCh37
NC_000002.10:g.206717989T=	NCBI36
NG_009248.1:g.19444A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233190.11:c.744A= MANE Select	ENSP00000233190.5:p.Thr248=
ENST00000233190.10:c.744A=	ENSP00000233190.5:p.Thr248=
ENST00000423725.5:c.573A=	ENSP00000397760.1:p.Thr191=
ENST00000432169.5:c.411A=	ENSP00000409689.1:p.Thr137=
ENST00000440274.5:c.636A=	ENSP00000409766.1:p.Thr212=
ENST00000449699.5:c.744A=	ENSP00000399912.1:p.Thr248=
ENST00000455934.6:c.786A=	ENSP00000392709.2:p.Thr262=
ENST00000457011.5:c.396A=	ENSP00000400976.1:p.Thr132=
NM_001199981.1:c.636A=	NP_001186910.1:p.Thr212=
NM_001199982.1:c.411A=	NP_001186911.1:p.Thr137=
NM_001199983.1:c.573A=	NP_001186912.1:p.Thr191=
NM_001199984.1:c.786A=	NP_001186913.1:p.Thr262=
NM_005006.6:c.744A=	NP_004997.4:p.Thr248=
XM_017004188.2:c.-16A=	XP_016859677.1:n.-16A=
NM_001199981.2:c.636A=	NP_001186910.1:p.Thr212=
NM_001199982.2:c.411A=	NP_001186911.1:p.Thr137=
NM_001199983.2:c.573A=	NP_001186912.1:p.Thr191=
NM_005006.7:c.744A= MANE Select	NP_004997.4:p.Thr248=
NM_001199984.2:c.786A=	NP_001186913.1:p.Thr262=