Canonical Allele Identifier: CA2602738250
Gene: GRHL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101644067_101644068del , CM000670.2:g.101644067_101644068del GRCh38
NC_000008.10:g.102656295_102656296del , CM000670.1:g.102656295_102656296del GRCh37
NC_000008.9:g.102725471_102725472del NCBI36
NG_011971.1:g.156628_156629del
NG_011971.2:g.156628_156629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646743.1:c.1518-64_1518-63del MANE Select ENSP00000495564.1:n.1518-64_1518-63del
ENST00000251808.7:c.1518-64_1518-63del ENSP00000251808.3:n.1518-64_1518-63del
ENST00000395927.1:c.1470-64_1470-63del ENSP00000379260.1:n.1470-64_1470-63del
ENST00000474338.1:n.160-64_160-63del
ENST00000517674.5:n.173-64_173-63del
NM_024915.3:c.1518-64_1518-63del NP_079191.2:n.1518-64_1518-63del
XM_011517305.1:c.1470-64_1470-63del XP_011515607.1:n.1470-64_1470-63del
XM_011517306.1:c.1470-64_1470-63del XP_011515608.1:n.1470-64_1470-63del
XM_011517307.1:c.1518-64_1518-63del XP_011515609.1:n.1518-64_1518-63del
NM_001330593.1:c.1470-64_1470-63del NP_001317522.1:n.1470-64_1470-63del
XM_011517306.3:c.1470-64_1470-63del XP_011515608.1:n.1470-64_1470-63del
XM_011517307.3:c.1518-64_1518-63del XP_011515609.1:n.1518-64_1518-63del
NM_001330593.2:c.1470-64_1470-63del NP_001317522.1:n.1470-64_1470-63del
NM_024915.4:c.1518-64_1518-63del MANE Select NP_079191.2:n.1518-64_1518-63del