Canonical Allele Identifier: CA2648114028

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991034-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991034G>C , CM000663.2:g.153991034G>C	GRCh38
NC_000001.10:g.153963510G>C , CM000663.1:g.153963510G>C	GRCh37
NC_000001.9:g.152230134G>C	NCBI36
NG_053102.2:g.5280G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.114G>C
ENST00000643794.1:c.127G>C	ENSP00000495765.1:p.Ala43Pro
ENST00000651669.1:c.7-81G>C MANE Select	ENSP00000499044.1:n.7-81G>C
ENST00000368567.4:c.7-81G>C	ENSP00000357555.4:n.7-81G>C
ENST00000392558.4:c.7-81G>C	ENSP00000376341.4:n.7-81G>C
ENST00000477151.1:n.161G>C
ENST00000493224.5:n.272G>C
NM_001030.4:c.7-81G>C	NP_001021.1:n.7-81G>C
NM_001030.6:c.7-81G>C MANE Select	NP_001021.1:n.7-81G>C
NM_001349946.1:c.-91G>C	NP_001336875.1:n.-91G>C
NM_001349947.1:c.-91G>C	NP_001336876.1:n.-91G>C
NM_001349946.2:c.-91G>C	NP_001336875.1:n.-91G>C
NM_001349947.2:c.-91G>C	NP_001336876.1:n.-91G>C