Canonical Allele Identifier: CA304392236
Gene: MATK HGNC NCBI

Linked Data

dbSNP Id: rs903928539

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797138C>A , CM000681.2:g.3797138C>A GRCh38
NC_000019.9:g.3797136C>A , CM000681.1:g.3797136C>A GRCh37
NC_000019.8:g.3748136C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4394G>T ENSP00000378485.1:n.-58+4394G>T
ENST00000590821.1:n.271+4394G>T
ENST00000590849.1:c.-52+4394G>T ENSP00000467992.1:n.-52+4394G>T
ENST00000590980.1:c.-58+4394G>T ENSP00000467472.1:n.-58+4394G>T
ENST00000592300.1:n.273-3737G>T
ENST00000592612.1:n.251-3740G>T
NM_002378.3:c.-58+4394G>T NP_002369.2:n.-58+4394G>T
XM_011528019.1:c.-58+4394G>T XP_011526321.1:n.-58+4394G>T
NM_002378.4:c.-58+4394G>T NP_002369.2:n.-58+4394G>T