Canonical Allele Identifier: CA413789278

Gene: CHM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85900663T>C , CM000685.2:g.85900663T>C	GRCh38
NC_000023.10:g.85155668T>C , CM000685.1:g.85155668T>C	GRCh37
NC_000023.9:g.85042324T>C	NCBI36
NG_009874.2:g.151900A>G , LRG_699:g.151900A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000390.4:c.1396A>G MANE Select	NP_000381.1:p.Thr466Ala
ENST00000357749.7:c.1396A>G MANE Select	ENSP00000350386.2:p.Thr466Ala
NM_000390.2:c.1396A>G , LRG_699t1:c.1396A>G	NP_000381.1:p.Thr466Ala
NM_000390.3:c.1396A>G	NP_000381.1:p.Thr466Ala
NM_001320959.1:c.952A>G	NP_001307888.1:p.Thr318Ala
NM_001362517.1:c.952A>G	NP_001349446.1:p.Thr318Ala
NM_001362518.1:c.952A>G	NP_001349447.1:p.Thr318Ala
NM_001362518.2:c.952A>G	NP_001349447.1:p.Thr318Ala
NM_001362519.1:c.952A>G	NP_001349448.1:p.Thr318Ala
ENST00000357749.6:c.1396A>G	ENSP00000350386.2:p.Thr466Ala
ENST00000467744.2:n.127-37569A>G
XM_006724615.2:c.1333A>G	XP_006724678.1:p.Thr445Ala
XM_011530839.1:c.952A>G	XP_011529141.1:p.Thr318Ala
XM_017029242.2:c.1396A>G	XP_016884731.1:p.Thr466Ala
XM_017029246.1:c.952A>G	XP_016884735.1:p.Thr318Ala
XM_024452331.1:c.952A>G	XP_024308099.1:p.Thr318Ala