Canonical Allele Identifier: CA655835120

Linked Data

dbSNP Id: rs1267322805

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599399A>G , CM000677.2:g.43599399A>G GRCh38
NC_000015.9:g.43891597A>G , CM000677.1:g.43891597A>G GRCh37
NC_000015.8:g.41678889A>G NCBI36
NG_011636.1:g.24402T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441322.6:c.*126A>G (CKMT1B) MANE Select ENSP00000413255.2:n.*126A>G
ENST00000300283.10:c.*126A>G (CKMT1B) ENSP00000300283.6:n.*126A>G
ENST00000411560.1:n.8A>G (CKMT1B)
ENST00000437534.3:c.*1300A>G (CKMT1B) ENSP00000416717.1:n.*1300A>G
ENST00000441322.5:c.*126A>G (CKMT1B) ENSP00000413255.1:n.*126A>G
ENST00000450892.6:c.*273T>C (STRC) ENSP00000401513.2:n.*273T>C
NM_020990.3:c.*126A>G (CKMT1B) NP_066270.1:n.*126A>G
XM_005254150.3:c.*126A>G (CKMT1B) XP_005254207.1:n.*126A>G
XM_011521194.1:c.*126A>G (CKMT1B) XP_011519496.1:n.*126A>G
XM_011521195.1:c.*126A>G (CKMT1B) XP_011519497.1:n.*126A>G
XM_011521196.1:c.*126A>G (CKMT1B) XP_011519498.1:n.*126A>G
XM_011521197.1:c.*126A>G (CKMT1B) XP_011519499.1:n.*126A>G
XM_011521198.1:c.*126A>G (CKMT1B) XP_011519500.1:n.*126A>G
XM_011521277.1:c.*273T>C (STRC) XP_011519579.1:n.*273T>C
XM_011521278.1:c.*273T>C (STRC) XP_011519580.1:n.*273T>C
XM_011521279.1:c.*273T>C (STRC) XP_011519581.1:n.*273T>C
NM_020990.4:c.*126A>G (CKMT1B) NP_066270.1:n.*126A>G
NR_135748.1:n.2835A>G (CKMT1B)
NR_135749.1:n.2815A>G (CKMT1B)
NR_135750.1:n.2786A>G (CKMT1B)
NR_135751.1:n.2675A>G (CKMT1B)
NR_135752.1:n.2442A>G (CKMT1B)
XM_005254150.4:c.*126A>G (CKMT1B) XP_005254207.1:n.*126A>G
XM_011521195.2:c.*126A>G (CKMT1B) XP_011519497.1:n.*126A>G
XM_011521197.2:c.*126A>G (CKMT1B) XP_011519499.1:n.*126A>G
XM_011521199.2:c.*126A>G (CKMT1B) XP_011519501.2:n.*126A>G
XM_017021902.1:c.*126A>G (CKMT1B) XP_016877391.1:n.*126A>G
NM_001375484.1:c.*126A>G (CKMT1B) MANE Select NP_001362413.1:n.*126A>G
NM_020990.5:c.*126A>G (CKMT1B) NP_066270.1:n.*126A>G
NR_135750.2:n.2786A>G (CKMT1B)