Canonical Allele Identifier: CA2319057225
Gene: MATK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797028G= , CM000681.2:g.3797028G= GRCh38
NC_000019.9:g.3797026G= , CM000681.1:g.3797026G= GRCh37
NC_000019.8:g.3748026G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395045.6:c.-58+4504C= ENSP00000378485.1:n.-58+4504C=
ENST00000590821.1:n.271+4504C=
ENST00000590849.1:c.-52+4504C= ENSP00000467992.1:n.-52+4504C=
ENST00000590980.1:c.-58+4504C= ENSP00000467472.1:n.-58+4504C=
ENST00000592300.1:n.273-3627C=
ENST00000592612.1:n.251-3630C=
NM_002378.3:c.-58+4504C= NP_002369.2:n.-58+4504C=
XM_011528019.1:c.-58+4504C= XP_011526321.1:n.-58+4504C=
NM_002378.4:c.-58+4504C= NP_002369.2:n.-58+4504C=
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