Canonical Allele Identifier: CA375229531
Gene: ASS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130480442G>T , CM000671.2:g.130480442G>T GRCh38
NC_000009.11:g.133355829G>T , CM000671.1:g.133355829G>T GRCh37
NC_000009.10:g.132345650G>T NCBI36
NG_011542.1:g.40736G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000352480.10:c.831G>T MANE Select ENSP00000253004.6:p.Lys277Asn
ENST00000352480.9:c.831G>T ENSP00000253004.6:p.Lys277Asn
ENST00000372386.6:n.102G>T
ENST00000372393.7:c.831G>T ENSP00000361469.2:p.Lys277Asn
ENST00000372394.5:c.831G>T ENSP00000361471.1:p.Lys277Asn
ENST00000470849.4:n.556G>T
ENST00000492400.5:n.340G>T
ENST00000493984.6:n.608G>T
NM_000050.4:c.831G>T NP_000041.2:p.Lys277Asn
NM_054012.3:c.831G>T NP_446464.1:p.Lys277Asn
XM_005272200.2:c.831G>T XP_005272257.1:p.Lys277Asn
XM_011518705.1:c.945G>T XP_011517007.1:p.Lys315Asn
XM_005272200.3:c.831G>T XP_005272257.1:p.Lys277Asn
XM_011518705.2:c.945G>T XP_011517007.1:p.Lys315Asn
XM_017014729.1:c.927G>T XP_016870218.1:p.Lys309Asn
NM_054012.4:c.831G>T MANE Select NP_446464.1:p.Lys277Asn