Canonical Allele Identifier: CA1806421625

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101644363_101644364delinsGT , CM000670.2:g.101644363_101644364delinsGT	GRCh38
NC_000008.10:g.102656591_102656592delinsGT , CM000670.1:g.102656591_102656592delinsGT	GRCh37
NC_000008.9:g.102725767_102725768delinsGT	NCBI36
NG_011971.1:g.156924_156925delinsGT
NG_011971.2:g.156924_156925delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.1612+138_1612+139delinsGT MANE Select	ENSP00000495564.1:n.1612+138_1612+139delinsGT
ENST00000251808.7:c.1612+138_1612+139delinsGT	ENSP00000251808.3:n.1612+138_1612+139delinsGT
ENST00000395927.1:c.1564+138_1564+139delinsGT	ENSP00000379260.1:n.1564+138_1564+139delinsGT
ENST00000474338.1:n.254+138_254+139delinsGT
ENST00000517674.5:n.267+138_267+139delinsGT
NM_024915.3:c.1612+138_1612+139delinsGT	NP_079191.2:n.1612+138_1612+139delinsGT
XM_011517305.1:c.1564+138_1564+139delinsGT	XP_011515607.1:n.1564+138_1564+139delinsGT
XM_011517306.1:c.1564+138_1564+139delinsGT	XP_011515608.1:n.1564+138_1564+139delinsGT
XM_011517307.1:c.1612+138_1612+139delinsGT	XP_011515609.1:n.1612+138_1612+139delinsGT
NM_001330593.1:c.1564+138_1564+139delinsGT	NP_001317522.1:n.1564+138_1564+139delinsGT
XM_011517306.3:c.1564+138_1564+139delinsGT	XP_011515608.1:n.1564+138_1564+139delinsGT
XM_011517307.3:c.1612+138_1612+139delinsGT	XP_011515609.1:n.1612+138_1612+139delinsGT
NM_001330593.2:c.1564+138_1564+139delinsGT	NP_001317522.1:n.1564+138_1564+139delinsGT
NM_024915.4:c.1612+138_1612+139delinsGT MANE Select	NP_079191.2:n.1612+138_1612+139delinsGT