Canonical Allele Identifier: CA389267766
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1285980987
gnomAD v2: 14-24728924-C-A
gnomAD v4: 14-24259718-C-A
MyVariant Identifiers: chr14:g.24728924C>A (hg19) chr14:g.24259718C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259718C>A , CM000676.2:g.24259718C>A GRCh38
NC_000014.8:g.24728924C>A , CM000676.1:g.24728924C>A GRCh37
NC_000014.7:g.23798764C>A NCBI36
NG_007150.1:g.8449G>T
NG_007150.2:g.8449G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.970G>T MANE Select ENSP00000206765.6:p.Val324Phe
ENST00000206765.10:c.970G>T ENSP00000206765.6:p.Val324Phe
ENST00000544573.5:c.-28-1330G>T ENSP00000439446.1:n.-28-1330G>T
ENST00000559136.1:c.43G>T ENSP00000453337.1:p.Val15Phe
NM_000359.2:c.970G>T NP_000350.1:p.Val324Phe
NM_000359.3:c.970G>T MANE Select NP_000350.1:p.Val324Phe
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