Canonical Allele Identifier: CA2580607695
Gene: MATK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797102C>G , CM000681.2:g.3797102C>G GRCh38
NC_000019.9:g.3797100C>G , CM000681.1:g.3797100C>G GRCh37
NC_000019.8:g.3748100C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4430G>C ENSP00000378485.1:n.-58+4430G>C
ENST00000590821.1:n.271+4430G>C
ENST00000590849.1:c.-52+4430G>C ENSP00000467992.1:n.-52+4430G>C
ENST00000590980.1:c.-58+4430G>C ENSP00000467472.1:n.-58+4430G>C
ENST00000592300.1:n.273-3701G>C
ENST00000592612.1:n.251-3704G>C
NM_002378.3:c.-58+4430G>C NP_002369.2:n.-58+4430G>C
XM_011528019.1:c.-58+4430G>C XP_011526321.1:n.-58+4430G>C
NM_002378.4:c.-58+4430G>C NP_002369.2:n.-58+4430G>C