Canonical Allele Identifier: CA3510138
Community Standard Title: NM_001012301.4(ARSI):c.1239C>T (p.Thr413=)
Gene: ARSI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.150297685G>A , CM000667.2:g.150297685G>A GRCh38
NC_000005.9:g.149677248G>A , CM000667.1:g.149677248G>A GRCh37
NC_000005.8:g.149657441G>A NCBI36
NG_051250.1:g.10278C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001012301.4:c.1239C>T MANE Select NP_001012301.1:p.Thr413=
ENST00000328668.8:c.1239C>T MANE Select ENSP00000333395.7:p.Thr413=
NM_001012301.2:c.1239C>T NP_001012301.1:p.Thr413=
NM_001012301.3:c.1239C>T NP_001012301.1:p.Thr413=
ENST00000328668.7:c.1239C>T ENSP00000333395.7:p.Thr413=
ENST00000515301.2:c.810C>T ENSP00000426879.2:p.Thr270=