Canonical Allele Identifier: CA2971382

Gene: CCDC158

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76362285G>A , CM000666.2:g.76362285G>A	GRCh38
NC_000004.11:g.77283438G>A , CM000666.1:g.77283438G>A	GRCh37
NC_000004.10:g.77502462G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001394954.1:c.1861C>T MANE Select	NP_001381883.1:p.Arg621Trp
ENST00000682701.1:c.1861C>T MANE Select	ENSP00000507278.1:p.Arg621Trp
NM_001042784.1:c.1861C>T	NP_001036249.1:p.Arg621Trp
ENST00000388914.7:c.1861C>T	ENSP00000373566.2:p.Arg621Trp
ENST00000504667.2:n.372C>T
XM_005262974.3:c.1861C>T	XP_005263031.1:p.Arg621Trp
XM_005262974.4:c.1861C>T	XP_005263031.1:p.Arg621Trp
XM_006714204.2:c.1861C>T	XP_006714267.1:p.Arg621Trp
XM_006714204.3:c.1861C>T	XP_006714267.1:p.Arg621Trp
XM_011531908.1:c.1861C>T	XP_011530210.1:p.Arg621Trp
XM_011531908.2:c.1861C>T	XP_011530210.1:p.Arg621Trp
XM_011531909.1:c.1861C>T	XP_011530211.1:p.Arg621Trp
XM_011531909.2:c.1861C>T	XP_011530211.1:p.Arg621Trp
XM_011531910.1:c.1861C>T	XP_011530212.1:p.Arg621Trp
XM_011531910.3:c.1861C>T	XP_011530212.1:p.Arg621Trp
XM_011531911.1:c.1861C>T	XP_011530213.1:p.Arg621Trp
XM_011531912.1:c.1861C>T	XP_011530214.1:p.Arg621Trp
XM_011531912.2:c.1861C>T	XP_011530214.1:p.Arg621Trp
XM_011531913.1:c.1861C>T	XP_011530215.1:p.Arg621Trp
XM_011531914.1:c.1861C>T	XP_011530216.1:p.Arg621Trp
XM_011531914.2:c.1861C>T	XP_011530216.1:p.Arg621Trp
XM_011531915.1:c.1861C>T	XP_011530217.1:p.Arg621Trp
XM_011531915.2:c.1861C>T	XP_011530217.1:p.Arg621Trp
XM_011531916.1:c.1615C>T	XP_011530218.1:p.Arg539Trp
XM_011531916.2:c.1615C>T	XP_011530218.1:p.Arg539Trp
XM_011531917.1:c.1615C>T	XP_011530219.1:p.Arg539Trp
XM_011531918.1:c.1423C>T	XP_011530220.1:p.Arg475Trp
XM_017008160.1:c.1861C>T	XP_016863649.1:p.Arg621Trp
XR_938729.1:n.2137C>T
XR_938729.2:n.2141C>T
XR_938730.1:n.2138C>T
XR_938730.2:n.2142C>T