Canonical Allele Identifier: CA1806376349

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543182_101543183delinsTA , CM000670.2:g.101543182_101543183delinsTA	GRCh38
NC_000008.10:g.102555410_102555411delinsTA , CM000670.1:g.102555410_102555411delinsTA	GRCh37
NC_000008.9:g.102624586_102624587delinsTA	NCBI36
NG_011971.1:g.55743_55744delinsTA
NG_011971.2:g.55743_55744delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.21-59_21-58delinsTA MANE Select	ENSP00000495564.1:n.21-59_21-58delinsTA
ENST00000251808.7:c.21-59_21-58delinsTA	ENSP00000251808.3:n.21-59_21-58delinsTA
ENST00000395927.1:c.-28-59_-28-58delinsTA	ENSP00000379260.1:n.-28-59_-28-58delinsTA
ENST00000472106.2:n.349-59_349-58delinsTA
NM_024915.3:c.21-59_21-58delinsTA	NP_079191.2:n.21-59_21-58delinsTA
XM_011517305.1:c.-28-59_-28-58delinsTA	XP_011515607.1:n.-28-59_-28-58delinsTA
XM_011517306.1:c.-28-59_-28-58delinsTA	XP_011515608.1:n.-28-59_-28-58delinsTA
XM_011517307.1:c.21-59_21-58delinsTA	XP_011515609.1:n.21-59_21-58delinsTA
NM_001330593.1:c.-28-59_-28-58delinsTA	NP_001317522.1:n.-28-59_-28-58delinsTA
XM_011517306.3:c.-28-59_-28-58delinsTA	XP_011515608.1:n.-28-59_-28-58delinsTA
XM_011517307.3:c.21-59_21-58delinsTA	XP_011515609.1:n.21-59_21-58delinsTA
NM_001330593.2:c.-28-59_-28-58delinsTA	NP_001317522.1:n.-28-59_-28-58delinsTA
NM_024915.4:c.21-59_21-58delinsTA MANE Select	NP_079191.2:n.21-59_21-58delinsTA