Canonical Allele Identifier: CA15255830
Gene: CMTM8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.32336779G>A , CM000665.2:g.32336779G>A GRCh38
NC_000003.11:g.32378271G>A , CM000665.1:g.32378271G>A GRCh37
NC_000003.10:g.32353275G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307526.4:c.148-20594G>A MANE Select ENSP00000307741.3:n.148-20594G>A
ENST00000307526.3:c.148-20594G>A ENSP00000307741.3:n.148-20594G>A
ENST00000458535.6:c.148-31093G>A ENSP00000412934.2:n.148-31093G>A
NM_178868.3:c.148-20594G>A NP_849199.2:n.148-20594G>A
XM_011533416.1:c.217-20594G>A XP_011531718.1:n.217-20594G>A
XM_011533417.1:c.148-31093G>A XP_011531719.1:n.148-31093G>A
NM_001320308.1:c.148-31093G>A NP_001307237.1:n.148-31093G>A
NM_178868.4:c.148-20594G>A NP_849199.2:n.148-20594G>A
XM_011533416.3:c.217-20594G>A XP_011531718.1:n.217-20594G>A
XM_017005779.1:c.19-20594G>A XP_016861268.1:n.19-20594G>A
XM_017005780.1:c.-73+1855G>A XP_016861269.1:n.-73+1855G>A
NM_178868.5:c.148-20594G>A MANE Select NP_849199.2:n.148-20594G>A
NM_001320308.2:c.148-31093G>A NP_001307237.1:n.148-31093G>A
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