Canonical Allele Identifier: CA2442458688

Gene: CHM

Linked Data

• dbSNP Id: rs1926199231
• gnomAD v4: X-85900614-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85900618del , CM000685.2:g.85900618del	GRCh38
NC_000023.10:g.85155623del , CM000685.1:g.85155623del	GRCh37
NC_000023.9:g.85042279del	NCBI36
NG_009874.2:g.151948del , LRG_699:g.151948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.1413+31del MANE Select	ENSP00000350386.2:n.1413+31del
ENST00000357749.6:c.1413+31del	ENSP00000350386.2:n.1413+31del
ENST00000467744.2:n.127-37521del
NM_000390.2:c.1413+31del , LRG_699t1:c.1413+31del	NP_000381.1:n.1413+31del
XM_006724615.2:c.1350+31del	XP_006724678.1:n.1350+31del
XM_011530839.1:c.969+31del	XP_011529141.1:n.969+31del
NM_000390.3:c.1413+31del	NP_000381.1:n.1413+31del
NM_001320959.1:c.969+31del	NP_001307888.1:n.969+31del
NM_001362517.1:c.969+31del	NP_001349446.1:n.969+31del
NM_001362518.1:c.969+31del	NP_001349447.1:n.969+31del
NM_001362519.1:c.969+31del	NP_001349448.1:n.969+31del
XM_017029242.2:c.1413+31del	XP_016884731.1:n.1413+31del
XM_017029246.1:c.969+31del	XP_016884735.1:n.969+31del
XM_024452331.1:c.969+31del	XP_024308099.1:n.969+31del
NM_000390.4:c.1413+31del MANE Select	NP_000381.1:n.1413+31del
NM_001362518.2:c.969+31del	NP_001349447.1:n.969+31del