Canonical Allele Identifier: CA2496487159

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206144506A= , CM000664.2:g.206144506A=	GRCh38
NC_000002.11:g.207009230A= , CM000664.1:g.207009230A=	GRCh37
NC_000002.10:g.206717475A=	NCBI36
NG_009248.1:g.19958T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.873-374T= MANE Select	ENSP00000233190.5:n.873-374T=
ENST00000233190.10:c.873-374T=	ENSP00000233190.5:n.873-374T=
ENST00000423725.5:c.702-374T=	ENSP00000397760.1:n.702-374T=
ENST00000432169.5:c.540-374T=	ENSP00000409689.1:n.540-374T=
ENST00000440274.5:c.765-374T=	ENSP00000409766.1:n.765-374T=
ENST00000449699.5:c.873-374T=	ENSP00000399912.1:n.873-374T=
ENST00000455934.6:c.915-374T=	ENSP00000392709.2:n.915-374T=
ENST00000457011.5:c.525-374T=	ENSP00000400976.1:n.525-374T=
NM_001199981.1:c.765-374T=	NP_001186910.1:n.765-374T=
NM_001199982.1:c.540-374T=	NP_001186911.1:n.540-374T=
NM_001199983.1:c.702-374T=	NP_001186912.1:n.702-374T=
NM_001199984.1:c.915-374T=	NP_001186913.1:n.915-374T=
NM_005006.6:c.873-374T=	NP_004997.4:n.873-374T=
XM_017004188.2:c.114-374T=	XP_016859677.1:n.114-374T=
NM_001199981.2:c.765-374T=	NP_001186910.1:n.765-374T=
NM_001199982.2:c.540-374T=	NP_001186911.1:n.540-374T=
NM_001199983.2:c.702-374T=	NP_001186912.1:n.702-374T=
NM_005006.7:c.873-374T= MANE Select	NP_004997.4:n.873-374T=
NM_001199984.2:c.915-374T=	NP_001186913.1:n.915-374T=