Canonical Allele Identifier: CA992788677
Gene: MATK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797230_3797231insTCT , CM000681.2:g.3797230_3797231insTCT GRCh38
NC_000019.9:g.3797228_3797229insTCT , CM000681.1:g.3797228_3797229insTCT GRCh37
NC_000019.8:g.3748228_3748229insTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395045.6:c.-58+4302_-58+4303insGAA ENSP00000378485.1:n.-58+4302_-58+4303insGAA
ENST00000590821.1:n.271+4302_271+4303insGAA
ENST00000590849.1:c.-52+4302_-52+4303insGAA ENSP00000467992.1:n.-52+4302_-52+4303insGAA
ENST00000590980.1:c.-58+4302_-58+4303insGAA ENSP00000467472.1:n.-58+4302_-58+4303insGAA
ENST00000592300.1:n.273-3829_273-3828insGAA
ENST00000592612.1:n.251-3832_251-3831insGAA
NM_002378.3:c.-58+4302_-58+4303insGAA NP_002369.2:n.-58+4302_-58+4303insGAA
XM_011528019.1:c.-58+4302_-58+4303insGAA XP_011526321.1:n.-58+4302_-58+4303insGAA
NM_002378.4:c.-58+4302_-58+4303insGAA NP_002369.2:n.-58+4302_-58+4303insGAA