Canonical Allele Identifier: CA1261985
Gene: RASAL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.178458299C>A , CM000663.2:g.178458299C>A GRCh38
NC_000001.10:g.178427434C>A , CM000663.1:g.178427434C>A GRCh37
NC_000001.9:g.176694057C>A NCBI36
NG_047109.1:g.369571C>A

Transcript Alleles

HGVS Amino-acid Change
NM_170692.4:c.3007C>A MANE Select NP_733793.2:p.Gln1003Lys
ENST00000367649.8:c.3007C>A MANE Select ENSP00000356621.3:p.Gln1003Lys
NM_004841.3:c.2584C>A NP_004832.1:p.Gln862Lys
NM_004841.5:c.2584C>A NP_004832.1:p.Gln862Lys
NM_170692.2:c.3007C>A NP_733793.2:p.Gln1003Lys
ENST00000367649.7:c.3007C>A ENSP00000356621.3:p.Gln1003Lys
ENST00000433130.2:c.1235C>A
ENST00000462775.5:c.2584C>A ENSP00000420558.1:p.Gln862Lys
ENST00000696605.1:c.3415C>A ENSP00000512749.1:p.Gln1139Lys
ENST00000696607.1:c.2572C>A ENSP00000512751.1:p.Gln858Lys
XM_005245622.2:c.2584C>A XP_005245679.1:p.Gln862Lys
XM_005245622.4:c.2584C>A XP_005245679.1:p.Gln862Lys
XM_011510166.1:c.3028C>A XP_011508468.1:p.Gln1010Lys
XM_011510166.2:c.3028C>A XP_011508468.1:p.Gln1010Lys
XM_011510167.1:c.3028C>A XP_011508469.1:p.Gln1010Lys
XM_011510167.2:c.3028C>A XP_011508469.1:p.Gln1010Lys
XM_011510168.1:c.3007C>A XP_011508470.1:p.Gln1003Lys
XM_011510169.1:c.2854C>A XP_011508471.1:p.Gln952Lys
XM_017002849.1:c.3415C>A XP_016858338.1:p.Gln1139Lys
XM_017002850.1:c.3415C>A XP_016858339.1:p.Gln1139Lys
XM_017002851.1:c.3394C>A XP_016858340.1:p.Gln1132Lys
XM_017002852.1:c.3394C>A XP_016858341.1:p.Gln1132Lys
XM_017002853.1:c.2860C>A XP_016858342.1:p.Gln954Lys
XM_017002854.1:c.2593C>A XP_016858343.1:p.Gln865Lys
XM_017002855.1:c.2572C>A XP_016858344.1:p.Gln858Lys