Canonical Allele Identifier: CA1881244316
Gene: ASS1 HGNC NCBI

Linked Data

dbSNP Id: rs556487021

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452144G>C , CM000671.2:g.130452144G>C GRCh38
NC_000009.11:g.133327531G>C , CM000671.1:g.133327531G>C GRCh37
NC_000009.10:g.132317352G>C NCBI36
NG_011542.1:g.12438G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.-5-80G>C MANE Select ENSP00000253004.6:n.-5-80G>C
ENST00000352480.9:c.-5-80G>C ENSP00000253004.6:n.-5-80G>C
ENST00000372393.7:c.-5-80G>C ENSP00000361469.2:n.-5-80G>C
ENST00000372394.5:c.-5-80G>C ENSP00000361471.1:n.-5-80G>C
ENST00000422569.5:c.-5-80G>C ENSP00000394212.1:n.-5-80G>C
NM_000050.4:c.-5-80G>C NP_000041.2:n.-5-80G>C
NM_054012.3:c.-5-80G>C NP_446464.1:n.-5-80G>C
XM_005272200.2:c.-5-80G>C XP_005272257.1:n.-5-80G>C
XM_011518705.1:c.110-80G>C XP_011517007.1:n.110-80G>C
XM_005272200.3:c.-5-80G>C XP_005272257.1:n.-5-80G>C
XM_011518705.2:c.110-80G>C XP_011517007.1:n.110-80G>C
XM_017014729.1:c.92-80G>C XP_016870218.1:n.92-80G>C
NM_054012.4:c.-5-80G>C MANE Select NP_446464.1:n.-5-80G>C