Canonical Allele Identifier: CA445402426
Gene: RASA1 HGNC NCBI

Linked Data

gnomAD v4: 5-87268926-C-T
MyVariant Identifiers: chr5:g.86564743C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268926C>T , CM000667.2:g.87268926C>T GRCh38
NC_000005.9:g.86564743C>T , CM000667.1:g.86564743C>T GRCh37
NC_000005.8:g.86600499C>T NCBI36
NG_011650.1:g.5593C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.475C>T MANE Select ENSP00000274376.6:p.Leu159=
ENST00000274376.10:c.475C>T ENSP00000274376.6:p.Leu159=
ENST00000515800.6:c.475C>T ENSP00000423395.2:p.Leu159=
NM_002890.2:c.475C>T NP_002881.1:p.Leu159=
NM_022650.2:c.-122C>T NP_072179.1:n.-122C>T
XM_011543525.1:c.475C>T XP_011541827.1:p.Leu159=
XM_011543526.1:c.475C>T XP_011541828.1:p.Leu159=
XM_011543527.1:c.475C>T XP_011541829.1:p.Leu159=
XM_011543525.2:c.475C>T XP_011541827.1:p.Leu159=
XM_011543527.3:c.475C>T XP_011541829.1:p.Leu159=
NM_002890.3:c.475C>T MANE Select NP_002881.1:p.Leu159=