Canonical Allele Identifier: CA1673644071

Gene: RGS17

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.153119944A>T , CM000668.2:g.153119944A>T	GRCh38
NC_000006.11:g.153441079A>T , CM000668.1:g.153441079A>T	GRCh37
NC_000006.10:g.153482772A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000206262.2:c.-26+11180T>A MANE Select	ENSP00000206262.1:n.-26+11180T>A
ENST00000206262.1:c.-26+11180T>A	ENSP00000206262.1:n.-26+11180T>A
NM_012419.4:c.-26+11180T>A	NP_036551.3:n.-26+11180T>A
XM_011535752.1:c.20+11095T>A	XP_011534054.1:n.20+11095T>A
XM_011535753.1:c.8+5140T>A	XP_011534055.1:n.8+5140T>A
XM_011535754.1:c.-26+10355T>A	XP_011534056.1:n.-26+10355T>A
XM_017010733.1:c.-26+11180T>A	XP_016866222.1:n.-26+11180T>A
NM_012419.5:c.-26+11180T>A MANE Select	NP_036551.3:n.-26+11180T>A