Canonical Allele Identifier: CA992788688
Gene: MATK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797230_3797232dup , CM000681.2:g.3797230_3797232dup GRCh38
NC_000019.9:g.3797228_3797230dup , CM000681.1:g.3797228_3797230dup GRCh37
NC_000019.8:g.3748228_3748230dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395045.6:c.-58+4300_-58+4302dup ENSP00000378485.1:n.-58+4300_-58+4302dup
ENST00000590821.1:n.271+4300_271+4302dup
ENST00000590849.1:c.-52+4300_-52+4302dup ENSP00000467992.1:n.-52+4300_-52+4302dup
ENST00000590980.1:c.-58+4300_-58+4302dup ENSP00000467472.1:n.-58+4300_-58+4302dup
ENST00000592300.1:n.273-3831_273-3829dup
ENST00000592612.1:n.251-3834_251-3832dup
NM_002378.3:c.-58+4300_-58+4302dup NP_002369.2:n.-58+4300_-58+4302dup
XM_011528019.1:c.-58+4300_-58+4302dup XP_011526321.1:n.-58+4300_-58+4302dup
NM_002378.4:c.-58+4300_-58+4302dup NP_002369.2:n.-58+4300_-58+4302dup