Canonical Allele Identifier: CA1226903962
Gene: GNPAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.231277738G= , CM000663.2:g.231277738G= GRCh38
NC_000001.10:g.231413484G= , CM000663.1:g.231413484G= GRCh37
NC_000001.9:g.229480107G= NCBI36
NG_008240.1:g.41566G=
NG_008240.2:g.41566G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366647.9:c.*196G= MANE Select ENSP00000355607.4:n.*196G=
ENST00000644483.1:c.*1925G= ENSP00000496537.1:n.*1925G=
ENST00000366647.8:c.*196G= ENSP00000355607.4:n.*196G=
NM_001316350.1:c.*196G= NP_001303279.1:n.*196G=
NM_014236.3:c.*196G= NP_055051.1:n.*196G=
XM_005273313.3:c.*196G= XP_005273370.1:n.*196G=
XM_011544303.1:c.*196G= XP_011542605.1:n.*196G=
XM_011544304.1:c.*196G= XP_011542606.1:n.*196G=
XM_005273313.4:c.*196G= XP_005273370.1:n.*196G=
XM_011544303.3:c.*196G= XP_011542605.1:n.*196G=
XM_011544304.2:c.*196G= XP_011542606.1:n.*196G=
NM_014236.4:c.*196G= MANE Select NP_055051.1:n.*196G=
NM_001316350.2:c.*196G= NP_001303279.1:n.*196G=