Canonical Allele Identifier: CA413786802

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85873159T>A , CM000685.2:g.85873159T>A	GRCh38
NC_000023.10:g.85128164T>A , CM000685.1:g.85128164T>A	GRCh37
NC_000023.9:g.85014820T>A	NCBI36
NG_009874.2:g.179404A>T , LRG_699:g.179404A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000390.4:c.1663A>T MANE Select	NP_000381.1:p.Arg555Ter
ENST00000357749.7:c.1663A>T MANE Select	ENSP00000350386.2:p.Arg555Ter
NM_000390.2:c.1663A>T , LRG_699t1:c.1663A>T	NP_000381.1:p.Arg555Ter
NM_000390.3:c.1663A>T	NP_000381.1:p.Arg555Ter
NM_001320959.1:c.1219A>T	NP_001307888.1:p.Arg407Ter
NM_001362517.1:c.1219A>T	NP_001349446.1:p.Arg407Ter
NM_001362518.1:c.1219A>T	NP_001349447.1:p.Arg407Ter
NM_001362518.2:c.1219A>T	NP_001349447.1:p.Arg407Ter
NM_001362519.1:c.1219A>T	NP_001349448.1:p.Arg407Ter
ENST00000357749.6:c.1663A>T	ENSP00000350386.2:p.Arg555Ter
ENST00000467744.2:n.127-10065A>T
XM_006724615.2:c.1600A>T	XP_006724678.1:p.Arg534Ter
XM_011530839.1:c.1219A>T	XP_011529141.1:p.Arg407Ter
XM_017029242.2:c.1663A>T	XP_016884731.1:p.Arg555Ter
XM_017029246.1:c.1219A>T	XP_016884735.1:p.Arg407Ter
XM_024452331.1:c.1219A>T	XP_024308099.1:p.Arg407Ter