Canonical Allele Identifier: CA445402357
Gene: RASA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.86564703T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87268886T>C , CM000667.2:g.87268886T>C GRCh38
NC_000005.9:g.86564703T>C , CM000667.1:g.86564703T>C GRCh37
NC_000005.8:g.86600459T>C NCBI36
NG_011650.1:g.5553T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.435T>C MANE Select ENSP00000274376.6:p.Pro145=
ENST00000274376.10:c.435T>C ENSP00000274376.6:p.Pro145=
ENST00000515800.6:c.435T>C ENSP00000423395.2:p.Pro145=
NM_002890.2:c.435T>C NP_002881.1:p.Pro145=
XM_011543525.1:c.435T>C XP_011541827.1:p.Pro145=
XM_011543526.1:c.435T>C XP_011541828.1:p.Pro145=
XM_011543527.1:c.435T>C XP_011541829.1:p.Pro145=
XM_011543525.2:c.435T>C XP_011541827.1:p.Pro145=
XM_011543527.3:c.435T>C XP_011541829.1:p.Pro145=
NM_002890.3:c.435T>C MANE Select NP_002881.1:p.Pro145=