Canonical Allele Identifier: CA1561548422
Gene: RASA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.87269011_87269012delinsAG , CM000667.2:g.87269011_87269012delinsAG GRCh38
NC_000005.9:g.86564828_86564829delinsAG , CM000667.1:g.86564828_86564829delinsAG GRCh37
NC_000005.8:g.86600584_86600585delinsAG NCBI36
NG_011650.1:g.5678_5679delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.539+21_539+22delinsAG MANE Select ENSP00000274376.6:n.539+21_539+22delinsAG...
ENST00000274376.10:c.539+21_539+22delinsAG ENSP00000274376.6:n.539+21_539+22delinsAG...
ENST00000456692.6:c.-37_-36delinsAG ENSP00000411221.2:n.-37_-36delinsAG
ENST00000506290.1:c.-50_-49delinsAG ENSP00000420905.1:n.-50_-49delinsAG
ENST00000512763.5:c.-134_-133delinsAG ENSP00000422008.1:n.-134_-133delinsAG
ENST00000515800.6:c.539+21_539+22delinsAG ENSP00000423395.2:n.539+21_539+22delinsAG...
NM_002890.2:c.539+21_539+22delinsAG NP_002881.1:n.539+21_539+22delinsAG
NM_022650.2:c.-37_-36delinsAG NP_072179.1:n.-37_-36delinsAG
XM_011543525.1:c.539+21_539+22delinsAG XP_011541827.1:n.539+21_539+22delinsAG
XM_011543526.1:c.539+21_539+22delinsAG XP_011541828.1:n.539+21_539+22delinsAG
XM_011543527.1:c.539+21_539+22delinsAG XP_011541829.1:n.539+21_539+22delinsAG
XM_011543525.2:c.539+21_539+22delinsAG XP_011541827.1:n.539+21_539+22delinsAG
XM_011543527.3:c.539+21_539+22delinsAG XP_011541829.1:n.539+21_539+22delinsAG
NM_002890.3:c.539+21_539+22delinsAG MANE Select NP_002881.1:n.539+21_539+22delinsAG
NM_022650.3:c.-37_-36delinsAG NP_072179.1:n.-37_-36delinsAG