Canonical Allele Identifier: CA360417625
Gene: RASA1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000274376.11:c.539+63G>T MANE Select ENSP00000274376.6:n.539+63G>T
ENST00000274376.10:c.539+63G>T ENSP00000274376.6:n.539+63G>T
ENST00000456692.6:c.6G>T ENSP00000411221.2:p.Lys2Asn
ENST00000506290.1:c.-8G>T ENSP00000420905.1:n.-8G>T
ENST00000512763.5:c.-92G>T ENSP00000422008.1:n.-92G>T
ENST00000515800.6:c.539+63G>T ENSP00000423395.2:n.539+63G>T
NM_002890.2:c.539+63G>T NP_002881.1:n.539+63G>T
NM_022650.2:c.6G>T NP_072179.1:p.Lys2Asn
XM_011543525.1:c.539+63G>T XP_011541827.1:n.539+63G>T
XM_011543526.1:c.539+63G>T XP_011541828.1:n.539+63G>T
XM_011543527.1:c.539+63G>T XP_011541829.1:n.539+63G>T
XM_011543525.2:c.539+63G>T XP_011541827.1:n.539+63G>T
XM_011543527.3:c.539+63G>T XP_011541829.1:n.539+63G>T
NM_002890.3:c.539+63G>T MANE Select NP_002881.1:n.539+63G>T
NM_022650.3:c.6G>T NP_072179.1:p.Lys2Asn