Canonical Allele Identifier: CA642998127

Gene: CHM

Linked Data

• dbSNP Id: rs1452534667
• gnomAD v2: X-85218667-T-TA
• MyVariant Identifiers: chrX:g.85218667_85218668insA (hg19) ; chrX:g.85963662_85963663insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963663dup , CM000685.2:g.85963663dup	GRCh38
NC_000023.10:g.85218668dup , CM000685.1:g.85218668dup	GRCh37
NC_000023.9:g.85105324dup	NCBI36
NG_009874.2:g.88900dup , LRG_699:g.88900dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.702+2dup MANE Select	ENSP00000350386.2:n.702+2dup
ENST00000357749.6:c.702+2dup	ENSP00000350386.2:n.702+2dup
ENST00000467744.2:n.126+63828dup
NM_000390.2:c.702+2dup , LRG_699t1:c.702+2dup	NP_000381.1:n.702+2dup
XM_006724615.2:c.639+2dup	XP_006724678.1:n.639+2dup
XM_011530839.1:c.258+2dup	XP_011529141.1:n.258+2dup
NM_000390.3:c.702+2dup	NP_000381.1:n.702+2dup
NM_001320959.1:c.258+2dup	NP_001307888.1:n.258+2dup
NM_001362517.1:c.258+2dup	NP_001349446.1:n.258+2dup
NM_001362518.1:c.258+2dup	NP_001349447.1:n.258+2dup
NM_001362519.1:c.258+2dup	NP_001349448.1:n.258+2dup
XM_017029242.2:c.702+2dup	XP_016884731.1:n.702+2dup
XM_017029246.1:c.258+2dup	XP_016884735.1:n.258+2dup
XM_024452331.1:c.258+2dup	XP_024308099.1:n.258+2dup
NM_000390.4:c.702+2dup MANE Select	NP_000381.1:n.702+2dup
NM_001362518.2:c.258+2dup	NP_001349447.1:n.258+2dup