Canonical Allele Identifier: CA844668491

Gene: GRHL2

Linked Data

• dbSNP Id: rs1428469024
• MyVariant Identifiers: chr8:g.102555406_102555410del (hg19) ; chr8:g.101543178_101543182del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543178_101543182del , CM000670.2:g.101543178_101543182del	GRCh38
NC_000008.10:g.102555406_102555410del , CM000670.1:g.102555406_102555410del	GRCh37
NC_000008.9:g.102624582_102624586del	NCBI36
NG_011971.1:g.55739_55743del
NG_011971.2:g.55739_55743del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.21-63_21-59del MANE Select	ENSP00000495564.1:n.21-63_21-59del
ENST00000251808.7:c.21-63_21-59del	ENSP00000251808.3:n.21-63_21-59del
ENST00000395927.1:c.-28-63_-28-59del	ENSP00000379260.1:n.-28-63_-28-59del
ENST00000472106.2:n.349-63_349-59del
NM_024915.3:c.21-63_21-59del	NP_079191.2:n.21-63_21-59del
XM_011517305.1:c.-28-63_-28-59del	XP_011515607.1:n.-28-63_-28-59del
XM_011517306.1:c.-28-63_-28-59del	XP_011515608.1:n.-28-63_-28-59del
XM_011517307.1:c.21-63_21-59del	XP_011515609.1:n.21-63_21-59del
NM_001330593.1:c.-28-63_-28-59del	NP_001317522.1:n.-28-63_-28-59del
XM_011517306.3:c.-28-63_-28-59del	XP_011515608.1:n.-28-63_-28-59del
XM_011517307.3:c.21-63_21-59del	XP_011515609.1:n.21-63_21-59del
NM_001330593.2:c.-28-63_-28-59del	NP_001317522.1:n.-28-63_-28-59del
NM_024915.4:c.21-63_21-59del MANE Select	NP_079191.2:n.21-63_21-59del