Canonical Allele Identifier: CA413785307

Gene: CHM

Linked Data

• gnomAD v4: X-85956306-A-G
• MyVariant Identifiers: chrX:g.85211311A>G (hg19) ; chrX:g.85956306A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85956306A>G , CM000685.2:g.85956306A>G	GRCh38
NC_000023.10:g.85211311A>G , CM000685.1:g.85211311A>G	GRCh37
NC_000023.9:g.85097967A>G	NCBI36
NG_009874.2:g.96257T>C , LRG_699:g.96257T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.1013T>C MANE Select	ENSP00000350386.2:p.Met338Thr
ENST00000357749.6:c.1013T>C	ENSP00000350386.2:p.Met338Thr
ENST00000467744.2:n.126+71185T>C
NM_000390.2:c.1013T>C , LRG_699t1:c.1013T>C	NP_000381.1:p.Met338Thr
XM_006724615.2:c.950T>C	XP_006724678.1:p.Met317Thr
XM_011530839.1:c.569T>C	XP_011529141.1:p.Met190Thr
NM_000390.3:c.1013T>C	NP_000381.1:p.Met338Thr
NM_001320959.1:c.569T>C	NP_001307888.1:p.Met190Thr
NM_001362517.1:c.569T>C	NP_001349446.1:p.Met190Thr
NM_001362518.1:c.569T>C	NP_001349447.1:p.Met190Thr
NM_001362519.1:c.569T>C	NP_001349448.1:p.Met190Thr
XM_017029242.2:c.1013T>C	XP_016884731.1:p.Met338Thr
XM_017029246.1:c.569T>C	XP_016884735.1:p.Met190Thr
XM_024452331.1:c.569T>C	XP_024308099.1:p.Met190Thr
NM_000390.4:c.1013T>C MANE Select	NP_000381.1:p.Met338Thr
NM_001362518.2:c.569T>C	NP_001349447.1:p.Met190Thr