Canonical Allele Identifier: CA2695205764

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177406030del , CM000667.2:g.177406030del GRCh38
NC_000005.9:g.176833031del , CM000667.1:g.176833031del GRCh37
NC_000005.8:g.176765637del NCBI36
NG_007568.1:g.8550del , LRG_145:g.8550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696192.1:c.150del (F12) ENSP00000512476.1:p.Phe51SerfsTer?
ENST00000696193.1:c.*74del (F12) ENSP00000512477.1:n.*74del
ENST00000696194.1:c.150del (F12) ENSP00000512478.1:p.Phe51SerfsTer?
ENST00000696195.1:n.2507del (F12)
ENST00000696200.1:n.253del (F12)
ENST00000696201.1:c.150del (F12) ENSP00000512482.1:p.Phe51SerfsTer?
ENST00000253496.4:c.150del (F12) MANE Select ENSP00000253496.3:p.Phe51SerfsTer?
ENST00000253496.3:c.150del (F12) ENSP00000253496.3:p.Phe51SerfsTer?
ENST00000502598.5:c.-45+2504del (GRK6) ENSP00000422873.1:n.-45+2504del
ENST00000506296.5:c.-45+1473del (GRK6) ENSP00000421055.1:n.-45+1473del
NM_000505.3:c.150del , LRG_145t1:c.150del (F12) NP_000496.2:p.Phe51SerfsTer?
XM_011534461.1:c.150del (F12) XP_011532763.1:p.Phe51SerfsTer?
XM_017009773.2:c.1417-5734del (SLC34A1) XP_016865262.1:n.1417-5734del
NM_000505.4:c.150del (F12) MANE Select NP_000496.2:p.Phe51SerfsTer?