Canonical Allele Identifier: CA2582641492
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399840_1399897dup , CM000681.2:g.1399840_1399897dup GRCh38
NC_000019.9:g.1399839_1399896dup , CM000681.1:g.1399839_1399896dup GRCh37
NC_000019.8:g.1350839_1350896dup NCBI36
NG_009785.1:g.6662_6719dup

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.228_285dup MANE Select ENSP00000252288.1:p.Phe96LysfsTer8
ENST00000447102.8:c.228_285dup ENSP00000403536.2:p.Phe96LysfsTer8
ENST00000640762.1:c.159_216dup ENSP00000492031.1:p.Phe73LysfsTer8
ENST00000252288.6:c.228_285dup ENSP00000252288.1:p.Phe96LysfsTer8
ENST00000447102.7:c.228_285dup ENSP00000403536.2:p.Phe96LysfsTer8
NM_000156.5:c.228_285dup NP_000147.1:p.Phe96LysfsTer8
NM_138924.2:c.228_285dup NP_620279.1:p.Phe96LysfsTer8
NM_000156.6:c.228_285dup MANE Select NP_000147.1:p.Phe96LysfsTer8
NM_138924.3:c.228_285dup NP_620279.1:p.Phe96LysfsTer8