Canonical Allele Identifier: CA1160113994
Gene: RPS6KA1 HGNC NCBI

Linked Data

dbSNP Id: rs2075930130

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26539416G>C , CM000663.2:g.26539416G>C GRCh38
NC_000001.10:g.26865907G>C , CM000663.1:g.26865907G>C GRCh37
NC_000001.9:g.26738494G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374168.7:c.108+2447G>C MANE Select ENSP00000363283.2:n.108+2447G>C
ENST00000374166.8:c.108+2447G>C ENSP00000363281.4:n.108+2447G>C
ENST00000374168.6:c.108+2447G>C ENSP00000363283.2:n.108+2447G>C
ENST00000524436.5:n.254+2447G>C
ENST00000525525.5:c.*95+2447G>C ENSP00000434616.1:n.*95+2447G>C
ENST00000526040.6:c.108+2447G>C ENSP00000436990.1:n.108+2447G>C
ENST00000526792.5:c.-169+2447G>C ENSP00000431651.1:n.-169+2447G>C
ENST00000529454.5:c.-52+2447G>C ENSP00000433039.1:n.-52+2447G>C
NM_002953.3:c.108+2447G>C NP_002944.2:n.108+2447G>C
XM_005245967.2:c.-169+2447G>C XP_005246024.1:n.-169+2447G>C
XM_011541898.1:c.-169+2447G>C XP_011540200.1:n.-169+2447G>C
XM_024448871.1:c.-169+2447G>C XP_024304639.1:n.-169+2447G>C
NM_002953.4:c.108+2447G>C MANE Select NP_002944.2:n.108+2447G>C