Canonical Allele Identifier: CA2609912766
Gene: MAT1A HGNC NCBI

Linked Data

gnomAD v4: 10-80273942-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273942C>G , CM000672.2:g.80273942C>G GRCh38
NC_000010.10:g.82033698C>G , CM000672.1:g.82033698C>G GRCh37
NC_000010.9:g.82023678C>G NCBI36
NG_008083.1:g.20737G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-59G>C MANE Select ENSP00000361287.3:n.1086-59G>C
ENST00000372213.7:c.1086-59G>C ENSP00000361287.3:n.1086-59G>C
ENST00000480845.1:n.318-59G>C
ENST00000485270.5:n.598-59G>C
NM_000429.2:c.1086-59G>C NP_000420.1:n.1086-59G>C
XM_005269842.3:c.1086-59G>C XP_005269899.1:n.1086-59G>C
XM_005269843.3:c.963-59G>C XP_005269900.1:n.963-59G>C
NM_000429.3:c.1086-59G>C MANE Select NP_000420.1:n.1086-59G>C
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