Canonical Allele Identifier: CA2781524018
Gene: GRHL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101543493del , CM000670.2:g.101543493del GRCh38
NC_000008.10:g.102555721del , CM000670.1:g.102555721del GRCh37
NC_000008.9:g.102624897del NCBI36
NG_011971.1:g.56054del
NG_011971.2:g.56054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646743.1:c.216+57del MANE Select ENSP00000495564.1:n.216+57del
ENST00000251808.7:c.216+57del ENSP00000251808.3:n.216+57del
ENST00000395927.1:c.168+57del ENSP00000379260.1:n.168+57del
ENST00000472106.2:n.601del
NM_024915.3:c.216+57del NP_079191.2:n.216+57del
XM_011517305.1:c.168+57del XP_011515607.1:n.168+57del
XM_011517306.1:c.168+57del XP_011515608.1:n.168+57del
XM_011517307.1:c.216+57del XP_011515609.1:n.216+57del
NM_001330593.1:c.168+57del NP_001317522.1:n.168+57del
XM_011517306.3:c.168+57del XP_011515608.1:n.168+57del
XM_011517307.3:c.216+57del XP_011515609.1:n.216+57del
NM_001330593.2:c.168+57del NP_001317522.1:n.168+57del
NM_024915.4:c.216+57del MANE Select NP_079191.2:n.216+57del