Canonical Allele Identifier: CA221723690

Gene: RAPSN

Linked Data

• dbSNP Id: rs1043342696
• gnomAD v2: 11-47470621-G-T
• gnomAD v3: 11-47449069-G-T
• gnomAD v4: 11-47449069-G-T
• MyVariant Identifiers: chr11:g.47470621G>T (hg19) ; chr11:g.47449069G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47449069G>T , CM000673.2:g.47449069G>T	GRCh38
NC_000011.9:g.47470621G>T , CM000673.1:g.47470621G>T	GRCh37
NC_000011.8:g.47427197G>T	NCBI36
NG_008312.1:g.5110C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.-105C>A MANE Select	ENSP00000298854.2:n.-105C>A
ENST00000298854.6:c.-105C>A	ENSP00000298854.2:n.-105C>A
ENST00000352508.7:c.-105C>A	ENSP00000298853.3:n.-105C>A
ENST00000524487.5:c.-105C>A	ENSP00000435551.2:n.-105C>A
ENST00000529341.1:c.-105C>A	ENSP00000431732.1:n.-105C>A
NM_005055.4:c.-105C>A	NP_005046.2:n.-105C>A
NM_032645.4:c.-105C>A	NP_116034.2:n.-105C>A
XM_005253042.2:c.-105C>A	XP_005253099.1:n.-105C>A
XM_005253043.2:c.-105C>A	XP_005253100.1:n.-105C>A
XM_011520252.1:c.-105C>A	XP_011518554.1:n.-105C>A
XM_011520253.1:c.-105C>A	XP_011518555.1:n.-105C>A
XM_005253042.3:c.-105C>A	XP_005253099.1:n.-105C>A
XM_005253043.3:c.-105C>A	XP_005253100.1:n.-105C>A
NM_005055.5:c.-105C>A MANE Select	NP_005046.2:n.-105C>A
NM_032645.5:c.-105C>A	NP_116034.2:n.-105C>A