Canonical Allele Identifier: CA2576548647
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398999_1399001del , CM000681.2:g.1398999_1399001del GRCh38
NC_000019.9:g.1398998_1399000del , CM000681.1:g.1398998_1399000del GRCh37
NC_000019.8:g.1349998_1350000del NCBI36
NG_009785.1:g.7553_7555del

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.485_487del MANE Select ENSP00000252288.1:p.Pro162_Gly163delinsAr...
ENST00000447102.8:c.485_487del ENSP00000403536.2:p.Pro162_Gly163delinsAr...
ENST00000591788.3:c.168_170del
ENST00000640164.1:n.318_320del
ENST00000640762.1:c.416_418del ENSP00000492031.1:p.Pro139_Gly140delinsAr...
ENST00000252288.6:c.485_487del ENSP00000252288.1:p.Pro162_Gly163delinsAr...
ENST00000447102.7:c.485_487del ENSP00000403536.2:p.Pro162_Gly163delinsAr...
ENST00000591788.2:c.170_172del ENSP00000466341.2:p.Pro57_Gly58delinsArg
NM_000156.5:c.485_487del NP_000147.1:p.Pro162_Gly163delinsArg
NM_138924.2:c.485_487del NP_620279.1:p.Pro162_Gly163delinsArg
NM_000156.6:c.485_487del MANE Select NP_000147.1:p.Pro162_Gly163delinsArg
NM_138924.3:c.485_487del NP_620279.1:p.Pro162_Gly163delinsArg