Canonical Allele Identifier: CA5283127
Community Standard Title: NM_054012.4(ASS1):c.19G>A (p.Val7Met)
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452247G>A , CM000671.2:g.130452247G>A GRCh38
NC_000009.11:g.133327634G>A , CM000671.1:g.133327634G>A GRCh37
NC_000009.10:g.132317455G>A NCBI36
NG_011542.1:g.12541G>A

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.19G>A MANE Select NP_446464.1:p.Val7Met
ENST00000352480.10:c.19G>A MANE Select ENSP00000253004.6:p.Val7Met
NM_000050.4:c.19G>A NP_000041.2:p.Val7Met
NM_054012.3:c.19G>A NP_446464.1:p.Val7Met
ENST00000352480.9:c.19G>A ENSP00000253004.6:p.Val7Met
ENST00000372393.7:c.19G>A ENSP00000361469.2:p.Val7Met
ENST00000372394.5:c.19G>A ENSP00000361471.1:p.Val7Met
ENST00000422569.5:c.19G>A ENSP00000394212.1:p.Val7Met
ENST00000443588.1:c.19G>A ENSP00000397785.1:p.Val7Met
XM_005272200.2:c.19G>A XP_005272257.1:p.Val7Met
XM_005272200.3:c.19G>A XP_005272257.1:p.Val7Met
XM_011518705.1:c.133G>A XP_011517007.1:p.Val45Met
XM_011518705.2:c.133G>A XP_011517007.1:p.Val45Met
XM_017014729.1:c.115G>A XP_016870218.1:p.Val39Met