Canonical Allele Identifier: CA1078449217
Gene: RASA1 HGNC NCBI

Linked Data

dbSNP Id: rs1753701855
gnomAD v3: 5-87269014-A-T
gnomAD v4: 5-87269014-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87269014A>T , CM000667.2:g.87269014A>T GRCh38
NC_000005.9:g.86564831A>T , CM000667.1:g.86564831A>T GRCh37
NC_000005.8:g.86600587A>T NCBI36
NG_011650.1:g.5681A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.539+24A>T MANE Select ENSP00000274376.6:n.539+24A>T
ENST00000274376.10:c.539+24A>T ENSP00000274376.6:n.539+24A>T
ENST00000456692.6:c.-34A>T ENSP00000411221.2:n.-34A>T
ENST00000506290.1:c.-47A>T ENSP00000420905.1:n.-47A>T
ENST00000512763.5:c.-131A>T ENSP00000422008.1:n.-131A>T
ENST00000515800.6:c.539+24A>T ENSP00000423395.2:n.539+24A>T
NM_002890.2:c.539+24A>T NP_002881.1:n.539+24A>T
NM_022650.2:c.-34A>T NP_072179.1:n.-34A>T
XM_011543525.1:c.539+24A>T XP_011541827.1:n.539+24A>T
XM_011543526.1:c.539+24A>T XP_011541828.1:n.539+24A>T
XM_011543527.1:c.539+24A>T XP_011541829.1:n.539+24A>T
XM_011543525.2:c.539+24A>T XP_011541827.1:n.539+24A>T
XM_011543527.3:c.539+24A>T XP_011541829.1:n.539+24A>T
NM_002890.3:c.539+24A>T MANE Select NP_002881.1:n.539+24A>T
NM_022650.3:c.-34A>T NP_072179.1:n.-34A>T