Canonical Allele Identifier: CA1806376471

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543494_101543495delinsTG , CM000670.2:g.101543494_101543495delinsTG	GRCh38
NC_000008.10:g.102555722_102555723delinsTG , CM000670.1:g.102555722_102555723delinsTG	GRCh37
NC_000008.9:g.102624898_102624899delinsTG	NCBI36
NG_011971.1:g.56055_56056delinsTG
NG_011971.2:g.56055_56056delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+58_216+59delinsTG MANE Select	ENSP00000495564.1:n.216+58_216+59delinsTG
ENST00000251808.7:c.216+58_216+59delinsTG	ENSP00000251808.3:n.216+58_216+59delinsTG
ENST00000395927.1:c.168+58_168+59delinsTG	ENSP00000379260.1:n.168+58_168+59delinsTG
ENST00000472106.2:n.602_603delinsTG
NM_024915.3:c.216+58_216+59delinsTG	NP_079191.2:n.216+58_216+59delinsTG
XM_011517305.1:c.168+58_168+59delinsTG	XP_011515607.1:n.168+58_168+59delinsTG
XM_011517306.1:c.168+58_168+59delinsTG	XP_011515608.1:n.168+58_168+59delinsTG
XM_011517307.1:c.216+58_216+59delinsTG	XP_011515609.1:n.216+58_216+59delinsTG
NM_001330593.1:c.168+58_168+59delinsTG	NP_001317522.1:n.168+58_168+59delinsTG
XM_011517306.3:c.168+58_168+59delinsTG	XP_011515608.1:n.168+58_168+59delinsTG
XM_011517307.3:c.216+58_216+59delinsTG	XP_011515609.1:n.216+58_216+59delinsTG
NM_001330593.2:c.168+58_168+59delinsTG	NP_001317522.1:n.168+58_168+59delinsTG
NM_024915.4:c.216+58_216+59delinsTG MANE Select	NP_079191.2:n.216+58_216+59delinsTG