Canonical Allele Identifier: CA645734
Gene: PAX7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.18691769A>G , CM000663.2:g.18691769A>G GRCh38
NC_000001.10:g.19018263A>G , CM000663.1:g.19018263A>G GRCh37
NC_000001.9:g.18890850A>G NCBI36
NG_023262.1:g.65764A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000420770.7:c.602A>G MANE Select ENSP00000403389.2:p.Glu201Gly
ENST00000375375.7:c.602A>G ENSP00000364524.3:p.Glu201Gly
ENST00000400661.3:c.596A>G ENSP00000383502.3:p.Glu199Gly
ENST00000420770.6:c.602A>G ENSP00000403389.2:p.Glu201Gly
NM_001135254.1:c.602A>G NP_001128726.1:p.Glu201Gly
NM_002584.2:c.602A>G NP_002575.1:p.Glu201Gly
NM_013945.2:c.596A>G NP_039236.1:p.Glu199Gly
NM_001135254.2:c.602A>G MANE Select NP_001128726.1:p.Glu201Gly
NM_002584.3:c.602A>G NP_002575.1:p.Glu201Gly
NM_013945.3:c.596A>G NP_039236.1:p.Glu199Gly