Canonical Allele Identifier: CA2695235283

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963897_85963900del , CM000685.2:g.85963897_85963900del	GRCh38
NC_000023.10:g.85218902_85218905del , CM000685.1:g.85218902_85218905del	GRCh37
NC_000023.9:g.85105558_85105561del	NCBI36
NG_009874.2:g.88666_88669del , LRG_699:g.88666_88669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.470_473del MANE Select	ENSP00000350386.2:p.Gln157LeufsTer10
ENST00000357749.6:c.470_473del	ENSP00000350386.2:p.Gln157LeufsTer10
ENST00000467744.2:n.126+63594_126+63597del
NM_000390.2:c.470_473del , LRG_699t1:c.470_473del	NP_000381.1:p.Gln157LeufsTer10
XM_006724615.2:c.407_410del	XP_006724678.1:p.Gln136LeufsTer10
XM_011530839.1:c.26_29del	XP_011529141.1:p.Gln9LeufsTer10
NM_000390.3:c.470_473del	NP_000381.1:p.Gln157LeufsTer10
NM_001320959.1:c.26_29del	NP_001307888.1:p.Gln9LeufsTer10
NM_001362517.1:c.26_29del	NP_001349446.1:p.Gln9LeufsTer10
NM_001362518.1:c.26_29del	NP_001349447.1:p.Gln9LeufsTer10
NM_001362519.1:c.26_29del	NP_001349448.1:p.Gln9LeufsTer10
XM_017029242.2:c.470_473del	XP_016884731.1:p.Gln157LeufsTer10
XM_017029246.1:c.26_29del	XP_016884735.1:p.Gln9LeufsTer10
XM_024452331.1:c.26_29del	XP_024308099.1:p.Gln9LeufsTer10
NM_000390.4:c.470_473del MANE Select	NP_000381.1:p.Gln157LeufsTer10
NM_001362518.2:c.26_29del	NP_001349447.1:p.Gln9LeufsTer10