Canonical Allele Identifier: CA2740657266
Gene: RASA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87269053G>A , CM000667.2:g.87269053G>A GRCh38
NC_000005.9:g.86564870G>A , CM000667.1:g.86564870G>A GRCh37
NC_000005.8:g.86600626G>A NCBI36
NG_011650.1:g.5720G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274376.11:c.539+63G>A MANE Select ENSP00000274376.6:n.539+63G>A
ENST00000274376.10:c.539+63G>A ENSP00000274376.6:n.539+63G>A
ENST00000456692.6:c.6G>A ENSP00000411221.2:p.Lys2=
ENST00000506290.1:c.-8G>A ENSP00000420905.1:n.-8G>A
ENST00000512763.5:c.-92G>A ENSP00000422008.1:n.-92G>A
ENST00000515800.6:c.539+63G>A ENSP00000423395.2:n.539+63G>A
NM_002890.2:c.539+63G>A NP_002881.1:n.539+63G>A
NM_022650.2:c.6G>A NP_072179.1:p.Lys2=
XM_011543525.1:c.539+63G>A XP_011541827.1:n.539+63G>A
XM_011543526.1:c.539+63G>A XP_011541828.1:n.539+63G>A
XM_011543527.1:c.539+63G>A XP_011541829.1:n.539+63G>A
XM_011543525.2:c.539+63G>A XP_011541827.1:n.539+63G>A
XM_011543527.3:c.539+63G>A XP_011541829.1:n.539+63G>A
NM_002890.3:c.539+63G>A MANE Select NP_002881.1:n.539+63G>A
NM_022650.3:c.6G>A NP_072179.1:p.Lys2=