Canonical Allele Identifier: CA2579220643
Gene: GRHL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101644127_101644128insACTA , CM000670.2:g.101644127_101644128insACTA GRCh38
NC_000008.10:g.102656355_102656356insACTA , CM000670.1:g.102656355_102656356insACTA GRCh37
NC_000008.9:g.102725531_102725532insACTA NCBI36
NG_011971.1:g.156688_156689insACTA
NG_011971.2:g.156688_156689insACTA

Transcript Alleles

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