Canonical Allele Identifier: CA1969387738

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441930_47441931delinsGA , CM000673.2:g.47441930_47441931delinsGA	GRCh38
NC_000011.9:g.47463482_47463483delinsGA , CM000673.1:g.47463482_47463483delinsGA	GRCh37
NC_000011.8:g.47420058_47420059delinsGA	NCBI36
NG_008312.1:g.12248_12249delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.691-10_691-9delinsTC MANE Select	ENSP00000298854.2:n.691-10_691-9delinsTC
ENST00000298854.6:c.691-10_691-9delinsTC	ENSP00000298854.2:n.691-10_691-9delinsTC
ENST00000352508.7:c.691-10_691-9delinsTC	ENSP00000298853.3:n.691-10_691-9delinsTC
ENST00000524487.5:c.532-10_532-9delinsTC	ENSP00000435551.2:n.532-10_532-9delinsTC
ENST00000529341.1:c.691-10_691-9delinsTC	ENSP00000431732.1:n.691-10_691-9delinsTC
NM_005055.4:c.691-10_691-9delinsTC	NP_005046.2:n.691-10_691-9delinsTC
NM_032645.4:c.691-10_691-9delinsTC	NP_116034.2:n.691-10_691-9delinsTC
XM_005253042.2:c.691-10_691-9delinsTC	XP_005253099.1:n.691-10_691-9delinsTC
XM_005253043.2:c.691-10_691-9delinsTC	XP_005253100.1:n.691-10_691-9delinsTC
XM_011520252.1:c.691-10_691-9delinsTC	XP_011518554.1:n.691-10_691-9delinsTC
XM_011520253.1:c.691-10_691-9delinsTC	XP_011518555.1:n.691-10_691-9delinsTC
XM_005253042.3:c.691-10_691-9delinsTC	XP_005253099.1:n.691-10_691-9delinsTC
XM_005253043.3:c.691-10_691-9delinsTC	XP_005253100.1:n.691-10_691-9delinsTC
NM_005055.5:c.691-10_691-9delinsTC MANE Select	NP_005046.2:n.691-10_691-9delinsTC
NM_032645.5:c.691-10_691-9delinsTC	NP_116034.2:n.691-10_691-9delinsTC