Canonical Allele Identifier: CA391111322

Gene: COA8 KLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103563070C>A , CM000676.2:g.103563070C>A	GRCh38
NC_000014.8:g.104029407C>A , CM000676.1:g.104029407C>A	GRCh37
NC_000014.7:g.103099160C>A	NCBI36
NG_041786.1:g.5114C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409074.8:c.69C>A (COA8) MANE Select	ENSP00000386485.3:p.Gly23=
ENST00000440963.2:c.69C>A (COA8)	ENSP00000388067.2:p.Gly23=
ENST00000458117.6:c.69C>A (COA8)	ENSP00000408525.2:p.Gly23=
ENST00000472726.3:c.69C>A	ENSP00000439065.2:p.Gly23=
ENST00000674165.1:c.108C>A (COA8)	ENSP00000501341.1:p.Gly36=
ENST00000409074.6:c.108C>A (COA8)	ENSP00000386485.2:p.Gly36=
ENST00000440963.1:c.106C>A (COA8)	ENSP00000388067.1:p.Leu36Met
ENST00000458117.5:c.92C>A (COA8)
ENST00000472726.2:c.108C>A	ENSP00000439065.1:p.Gly36=
ENST00000489117.5:c.18C>A (COA8)	ENSP00000451788.1:p.Gly6=
ENST00000554625.5:n.89C>A (COA8)
ENST00000556253.6:c.69C>A (COA8)	ENSP00000451874.2:p.Gly23=
ENST00000557172.5:c.-2+1086C>A (KLC1)	ENSP00000450786.1:n.-2+1086C>A
NM_001302652.1:c.108C>A (COA8)	NP_001289581.1:p.Gly36=
NM_001302653.1:c.108C>A (COA8)	NP_001289582.1:p.Gly36=
NM_001302654.1:c.108C>A (COA8)	NP_001289583.1:p.Gly36=
NM_032374.4:c.108C>A (COA8)	NP_115750.2:p.Gly36=
NR_126431.1:n.114C>A (COA8)
NR_126432.1:n.114C>A (COA8)
NM_001302652.2:c.69C>A (COA8)	NP_001289581.2:p.Gly23=
NM_001302653.2:c.69C>A (COA8)	NP_001289582.2:p.Gly23=
NM_001302654.2:c.69C>A (COA8)	NP_001289583.2:p.Gly23=
NM_001370595.2:c.69C>A (COA8) MANE Select	NP_001357524.1:p.Gly23=
NR_126431.2:n.111C>A (COA8)
NR_126432.2:n.111C>A (COA8)