Canonical Allele Identifier: CA1188974224
Gene: RAP1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111565011A= , CM000663.2:g.111565011A= GRCh38
NC_000001.10:g.112107633A= , CM000663.1:g.112107633A= GRCh37
NC_000001.9:g.111909156A= NCBI36
NG_032119.1:g.3965T= , LRG_424:g.3965T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356415.5:c.-28+22502A= ENSP00000348786.1:n.-28+22502A=
XM_017001964.1:c.-28+22502A= XP_016857453.1:n.-28+22502A=
NM_001370216.1:c.-28+22502A= NP_001357145.1:n.-28+22502A=
NM_001370216.2:c.-28+22502A= NP_001357145.1:n.-28+22502A=
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