Canonical Allele Identifier: CA992788603
Gene: MATK HGNC NCBI

Linked Data

dbSNP Id: rs2037601321
gnomAD v3: 19-3797007-C-A
gnomAD v4: 19-3797007-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797007C>A , CM000681.2:g.3797007C>A GRCh38
NC_000019.9:g.3797005C>A , CM000681.1:g.3797005C>A GRCh37
NC_000019.8:g.3748005C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4525G>T ENSP00000378485.1:n.-58+4525G>T
ENST00000590821.1:n.271+4525G>T
ENST00000590849.1:c.-52+4525G>T ENSP00000467992.1:n.-52+4525G>T
ENST00000590980.1:c.-58+4525G>T ENSP00000467472.1:n.-58+4525G>T
ENST00000592300.1:n.273-3606G>T
ENST00000592612.1:n.251-3609G>T
NM_002378.3:c.-58+4525G>T NP_002369.2:n.-58+4525G>T
XM_011528019.1:c.-58+4525G>T XP_011526321.1:n.-58+4525G>T
NM_002378.4:c.-58+4525G>T NP_002369.2:n.-58+4525G>T