Canonical Allele Identifier: CA1806376451

Gene: GRHL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.101543457_101543462delinsTTTCTC , CM000670.2:g.101543457_101543462delinsTTTCTC	GRCh38
NC_000008.10:g.102555685_102555690delinsTTTCTC , CM000670.1:g.102555685_102555690delinsTTTCTC	GRCh37
NC_000008.9:g.102624861_102624866delinsTTTCTC	NCBI36
NG_011971.1:g.56018_56023delinsTTTCTC
NG_011971.2:g.56018_56023delinsTTTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646743.1:c.216+21_216+26delinsTTTCTC MANE Select	ENSP00000495564.1:n.216+21_216+26delinsTTTCTC
ENST00000251808.7:c.216+21_216+26delinsTTTCTC	ENSP00000251808.3:n.216+21_216+26delinsTTTCTC
ENST00000395927.1:c.168+21_168+26delinsTTTCTC	ENSP00000379260.1:n.168+21_168+26delinsTTTCTC
ENST00000472106.2:n.565_570delinsTTTCTC
NM_024915.3:c.216+21_216+26delinsTTTCTC	NP_079191.2:n.216+21_216+26delinsTTTCTC
XM_011517305.1:c.168+21_168+26delinsTTTCTC	XP_011515607.1:n.168+21_168+26delinsTTTCTC
XM_011517306.1:c.168+21_168+26delinsTTTCTC	XP_011515608.1:n.168+21_168+26delinsTTTCTC
XM_011517307.1:c.216+21_216+26delinsTTTCTC	XP_011515609.1:n.216+21_216+26delinsTTTCTC
NM_001330593.1:c.168+21_168+26delinsTTTCTC	NP_001317522.1:n.168+21_168+26delinsTTTCTC
XM_011517306.3:c.168+21_168+26delinsTTTCTC	XP_011515608.1:n.168+21_168+26delinsTTTCTC
XM_011517307.3:c.216+21_216+26delinsTTTCTC	XP_011515609.1:n.216+21_216+26delinsTTTCTC
NM_001330593.2:c.168+21_168+26delinsTTTCTC	NP_001317522.1:n.168+21_168+26delinsTTTCTC
NM_024915.4:c.216+21_216+26delinsTTTCTC MANE Select	NP_079191.2:n.216+21_216+26delinsTTTCTC