Canonical Allele Identifier: CA2319057209
Gene: MATK HGNC NCBI

Linked Data

dbSNP Id: rs2037601239

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797003G>T , CM000681.2:g.3797003G>T GRCh38
NC_000019.9:g.3797001G>T , CM000681.1:g.3797001G>T GRCh37
NC_000019.8:g.3748001G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4529C>A ENSP00000378485.1:n.-58+4529C>A
ENST00000590821.1:n.271+4529C>A
ENST00000590849.1:c.-52+4529C>A ENSP00000467992.1:n.-52+4529C>A
ENST00000590980.1:c.-58+4529C>A ENSP00000467472.1:n.-58+4529C>A
ENST00000592300.1:n.273-3602C>A
ENST00000592612.1:n.251-3605C>A
NM_002378.3:c.-58+4529C>A NP_002369.2:n.-58+4529C>A
XM_011528019.1:c.-58+4529C>A XP_011526321.1:n.-58+4529C>A
NM_002378.4:c.-58+4529C>A NP_002369.2:n.-58+4529C>A