Canonical Allele Identifier: CA689969

Gene: GRHL3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24337137C>T , CM000663.2:g.24337137C>T	GRCh38
NC_000001.10:g.24663627C>T , CM000663.1:g.24663627C>T	GRCh37
NC_000001.9:g.24536214C>T	NCBI36
NG_009308.1:g.22747C>T
NG_009308.2:g.22747C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_198173.3:c.672C>T MANE Select	NP_937816.1:p.Tyr224=
ENST00000361548.9:c.672C>T MANE Select	ENSP00000354943.5:p.Tyr224=
NM_001195010.1:c.534C>T	NP_001181939.1:p.Tyr178=
NM_001195010.2:c.534C>T	NP_001181939.1:p.Tyr178=
NM_021180.3:c.687C>T	NP_067003.2:p.Tyr229=
NM_021180.4:c.687C>T	NP_067003.2:p.Tyr229=
NM_198173.2:c.672C>T	NP_937816.1:p.Tyr224=
NM_198174.2:c.672C>T	NP_937817.3:p.Tyr224=
NM_198174.3:c.672C>T	NP_937817.3:p.Tyr224=
ENST00000236255.4:c.687C>T	ENSP00000236255.4:p.Tyr229=
ENST00000350501.9:c.672C>T	ENSP00000288955.5:p.Tyr224=
ENST00000356046.6:c.534C>T	ENSP00000348333.2:p.Tyr178=
ENST00000361548.8:c.672C>T	ENSP00000354943.4:p.Tyr224=
ENST00000461318.2:c.672C>T	ENSP00000508789.1:p.Tyr224=
ENST00000524724.6:c.534C>T	ENSP00000431290.2:p.Tyr178=
ENST00000528064.5:c.*341C>T	ENSP00000435130.1:n.*341C>T
ENST00000528064.6:c.393C>T	ENSP00000435130.2:p.Tyr131=
ENST00000689444.1:c.534C>T	ENSP00000509040.1:p.Tyr178=
ENST00000690803.1:c.393C>T	ENSP00000510783.1:p.Tyr131=
ENST00000692334.1:c.393C>T	ENSP00000509790.1:p.Tyr131=
XM_011541869.1:c.534C>T	XP_011540171.1:p.Tyr178=
XM_011541870.1:c.393C>T	XP_011540172.1:p.Tyr131=
XM_011541870.2:c.393C>T	XP_011540172.1:p.Tyr131=