Canonical Allele Identifier: CA2319057252
Gene: MATK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797086T= , CM000681.2:g.3797086T= GRCh38
NC_000019.9:g.3797084T= , CM000681.1:g.3797084T= GRCh37
NC_000019.8:g.3748084T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4446A= ENSP00000378485.1:n.-58+4446A=
ENST00000590821.1:n.271+4446A=
ENST00000590849.1:c.-52+4446A= ENSP00000467992.1:n.-52+4446A=
ENST00000590980.1:c.-58+4446A= ENSP00000467472.1:n.-58+4446A=
ENST00000592300.1:n.273-3685A=
ENST00000592612.1:n.251-3688A=
NM_002378.3:c.-58+4446A= NP_002369.2:n.-58+4446A=
XM_011528019.1:c.-58+4446A= XP_011526321.1:n.-58+4446A=
NM_002378.4:c.-58+4446A= NP_002369.2:n.-58+4446A=