Canonical Allele Identifier: CA375229525
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130480440A>G , CM000671.2:g.130480440A>G GRCh38
NC_000009.11:g.133355827A>G , CM000671.1:g.133355827A>G GRCh37
NC_000009.10:g.132345648A>G NCBI36
NG_011542.1:g.40734A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.829A>G MANE Select ENSP00000253004.6:p.Lys277Glu
ENST00000352480.9:c.829A>G ENSP00000253004.6:p.Lys277Glu
ENST00000372386.6:n.100A>G
ENST00000372393.7:c.829A>G ENSP00000361469.2:p.Lys277Glu
ENST00000372394.5:c.829A>G ENSP00000361471.1:p.Lys277Glu
ENST00000470849.4:n.554A>G
ENST00000492400.5:n.338A>G
ENST00000493984.6:n.606A>G
NM_000050.4:c.829A>G NP_000041.2:p.Lys277Glu
NM_054012.3:c.829A>G NP_446464.1:p.Lys277Glu
XM_005272200.2:c.829A>G XP_005272257.1:p.Lys277Glu
XM_011518705.1:c.943A>G XP_011517007.1:p.Lys315Glu
XM_005272200.3:c.829A>G XP_005272257.1:p.Lys277Glu
XM_011518705.2:c.943A>G XP_011517007.1:p.Lys315Glu
XM_017014729.1:c.925A>G XP_016870218.1:p.Lys309Glu
NM_054012.4:c.829A>G MANE Select NP_446464.1:p.Lys277Glu