Canonical Allele Identifier: CA210321138

Gene: MAT1A

Linked Data

• dbSNP Id: rs557681544
• gnomAD v3: 10-80273970-G-A
• gnomAD v4: 10-80273970-G-A
• MyVariant Identifiers: chr10:g.82033726G>A (hg19) ; chr10:g.80273970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80273970G>A , CM000672.2:g.80273970G>A	GRCh38
NC_000010.10:g.82033726G>A , CM000672.1:g.82033726G>A	GRCh37
NC_000010.9:g.82023706G>A	NCBI36
NG_008083.1:g.20709C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.1086-87C>T MANE Select	ENSP00000361287.3:n.1086-87C>T
ENST00000372213.7:c.1086-87C>T	ENSP00000361287.3:n.1086-87C>T
ENST00000480845.1:n.318-87C>T
ENST00000485270.5:n.598-87C>T
NM_000429.2:c.1086-87C>T	NP_000420.1:n.1086-87C>T
XM_005269842.3:c.1086-87C>T	XP_005269899.1:n.1086-87C>T
XM_005269843.3:c.963-87C>T	XP_005269900.1:n.963-87C>T
NM_000429.3:c.1086-87C>T MANE Select	NP_000420.1:n.1086-87C>T