Canonical Allele Identifier: CA1940036397
Gene: GRK5 HGNC NCBI

Linked Data

dbSNP Id: rs1850681799

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119326510_119326511del , CM000672.2:g.119326510_119326511del GRCh38
NC_000010.10:g.121086022_121086023del , CM000672.1:g.121086022_121086023del GRCh37
NC_000010.9:g.121076012_121076013del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392870.3:c.53-6_53-5del MANE Select ENSP00000376609.2:n.53-6_53-5del
ENST00000392870.2:c.53-6_53-5del ENSP00000376609.2:n.53-6_53-5del
NM_005308.2:c.53-6_53-5del NP_005299.1:n.53-6_53-5del
XM_005269707.1:c.53-6_53-5del XP_005269764.1:n.53-6_53-5del
XM_005269708.1:c.53-54305_53-54304del XP_005269765.1:n.53-54305_53-54304del
XM_005269707.2:c.53-6_53-5del XP_005269764.1:n.53-6_53-5del
NM_005308.3:c.53-6_53-5del MANE Select NP_005299.1:n.53-6_53-5del