Canonical Allele Identifier: CA445402196
Gene: RASA1 HGNC NCBI

Linked Data

gnomAD v4: 5-87268790-C-T
MyVariant Identifiers: chr5:g.86564607C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268790C>T , CM000667.2:g.87268790C>T GRCh38
NC_000005.9:g.86564607C>T , CM000667.1:g.86564607C>T GRCh37
NC_000005.8:g.86600363C>T NCBI36
NG_011650.1:g.5457C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.339C>T MANE Select ENSP00000274376.6:p.Asp113=
ENST00000274376.10:c.339C>T ENSP00000274376.6:p.Asp113=
ENST00000515800.6:c.339C>T ENSP00000423395.2:p.Asp113=
NM_002890.2:c.339C>T NP_002881.1:p.Asp113=
XM_011543525.1:c.339C>T XP_011541827.1:p.Asp113=
XM_011543526.1:c.339C>T XP_011541828.1:p.Asp113=
XM_011543527.1:c.339C>T XP_011541829.1:p.Asp113=
XM_011543525.2:c.339C>T XP_011541827.1:p.Asp113=
XM_011543527.3:c.339C>T XP_011541829.1:p.Asp113=
NM_002890.3:c.339C>T MANE Select NP_002881.1:p.Asp113=