Canonical Allele Identifier: CA2496479122

Gene: NDUFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.206127913T= , CM000664.2:g.206127913T=	GRCh38
NC_000002.11:g.206992637T= , CM000664.1:g.206992637T=	GRCh37
NC_000002.10:g.206700882T=	NCBI36
NG_009248.1:g.36551A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233190.11:c.1768A= MANE Select	ENSP00000233190.5:p.Thr590=
ENST00000233190.10:c.1768A=	ENSP00000233190.5:p.Thr590=
ENST00000423725.5:c.1597A=	ENSP00000397760.1:p.Thr533=
ENST00000432169.5:c.1435A=	ENSP00000409689.1:p.Thr479=
ENST00000440274.5:c.1660A=	ENSP00000409766.1:p.Thr554=
ENST00000449699.5:c.1768A=	ENSP00000399912.1:p.Thr590=
ENST00000455934.6:c.1810A=	ENSP00000392709.2:p.Thr604=
ENST00000457011.5:c.1420A=	ENSP00000400976.1:p.Thr474=
ENST00000498520.1:n.240A=
NM_001199981.1:c.1660A=	NP_001186910.1:p.Thr554=
NM_001199982.1:c.1435A=	NP_001186911.1:p.Thr479=
NM_001199983.1:c.1597A=	NP_001186912.1:p.Thr533=
NM_001199984.1:c.1810A=	NP_001186913.1:p.Thr604=
NM_005006.6:c.1768A=	NP_004997.4:p.Thr590=
XM_017004188.2:c.1009A=	XP_016859677.1:p.Thr337=
NM_001199981.2:c.1660A=	NP_001186910.1:p.Thr554=
NM_001199982.2:c.1435A=	NP_001186911.1:p.Thr479=
NM_001199983.2:c.1597A=	NP_001186912.1:p.Thr533=
NM_005006.7:c.1768A= MANE Select	NP_004997.4:p.Thr590=
NM_001199984.2:c.1810A=	NP_001186913.1:p.Thr604=