Canonical Allele Identifier: CA1969379589
Gene: RAPSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47448924A= , CM000673.2:g.47448924A= GRCh38
NC_000011.9:g.47470476A= , CM000673.1:g.47470476A= GRCh37
NC_000011.8:g.47427052A= NCBI36
NG_008312.1:g.5255T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298854.7:c.41T= MANE Select ENSP00000298854.2:p.Leu14=
ENST00000298854.6:c.41T= ENSP00000298854.2:p.Leu14=
ENST00000352508.7:c.41T= ENSP00000298853.3:p.Leu14=
ENST00000524487.5:c.41T= ENSP00000435551.2:p.Leu14=
ENST00000529341.1:c.41T= ENSP00000431732.1:p.Leu14=
NM_005055.4:c.41T= NP_005046.2:p.Leu14=
NM_032645.4:c.41T= NP_116034.2:p.Leu14=
XM_005253042.2:c.41T= XP_005253099.1:p.Leu14=
XM_005253043.2:c.41T= XP_005253100.1:p.Leu14=
XM_011520252.1:c.41T= XP_011518554.1:p.Leu14=
XM_011520253.1:c.41T= XP_011518555.1:p.Leu14=
XM_005253042.3:c.41T= XP_005253099.1:p.Leu14=
XM_005253043.3:c.41T= XP_005253100.1:p.Leu14=
NM_005055.5:c.41T= MANE Select NP_005046.2:p.Leu14=
NM_032645.5:c.41T= NP_116034.2:p.Leu14=