Canonical Allele Identifier: CA1243164621
Gene: RASGRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.33457584T= , CM000664.2:g.33457584T= GRCh38
NC_000002.11:g.33682651T= , CM000664.1:g.33682651T= GRCh37
NC_000002.10:g.33536155T= NCBI36
NG_053077.1:g.26237T=

Transcript Alleles

HGVS Amino-acid change
ENST00000402538.7:c.-261+9641T= ENSP00000385886.3:n.-261+9641T=
ENST00000479528.5:n.149+9641T=
ENST00000484909.5:n.390+9641T=
ENST00000497723.6:n.303+9641T=
NM_170672.2:c.-261+9641T= NP_733772.1:n.-261+9641T=
XM_011532746.1:c.-159+9641T= XP_011531048.1:n.-159+9641T=
NM_001349975.1:c.-383+9641T= NP_001336904.1:n.-383+9641T=
NM_001349978.1:c.-261+9641T= NP_001336907.1:n.-261+9641T=
XM_011532746.3:c.-159+9641T= XP_011531048.1:n.-159+9641T=
XM_017003759.2:c.-1635+9641T= XP_016859248.1:n.-1635+9641T=
NM_001349975.2:c.-383+9641T= NP_001336904.1:n.-383+9641T=
NM_001349978.2:c.-261+9641T= NP_001336907.1:n.-261+9641T=
NM_170672.3:c.-261+9641T= NP_733772.1:n.-261+9641T=