Canonical Allele Identifier: CA339049167

Gene: GRHL3

Linked Data

• MyVariant Identifiers: chr1:g.24673973G>C (hg19) ; chr1:g.24347483G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24347483G>C , CM000663.2:g.24347483G>C	GRCh38
NC_000001.10:g.24673973G>C , CM000663.1:g.24673973G>C	GRCh37
NC_000001.9:g.24546560G>C	NCBI36
NG_009308.1:g.33093G>C
NG_009308.2:g.33093G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524724.6:c.1421G>C	ENSP00000431290.2:p.Arg474Pro
ENST00000528064.6:c.1280G>C	ENSP00000435130.2:p.Arg427Pro
ENST00000689444.1:c.1421G>C	ENSP00000509040.1:p.Arg474Pro
ENST00000690803.1:c.1280G>C	ENSP00000510783.1:p.Arg427Pro
ENST00000692334.1:c.1280G>C	ENSP00000509790.1:p.Arg427Pro
ENST00000361548.9:c.1559G>C MANE Select	ENSP00000354943.5:p.Arg520Pro
ENST00000236255.4:c.1574G>C	ENSP00000236255.4:p.Arg525Pro
ENST00000350501.9:c.1559G>C	ENSP00000288955.5:p.Arg520Pro
ENST00000356046.6:c.1421G>C	ENSP00000348333.2:p.Arg474Pro
ENST00000361548.8:c.1559G>C	ENSP00000354943.4:p.Arg520Pro
ENST00000528064.5:c.*1228G>C	ENSP00000435130.1:n.*1228G>C
NM_001195010.1:c.1421G>C	NP_001181939.1:p.Arg474Pro
NM_021180.3:c.1574G>C	NP_067003.2:p.Arg525Pro
NM_198173.2:c.1559G>C	NP_937816.1:p.Arg520Pro
NM_198174.2:c.1559G>C	NP_937817.3:p.Arg520Pro
XM_011541869.1:c.1421G>C	XP_011540171.1:p.Arg474Pro
XM_011541870.1:c.1280G>C	XP_011540172.1:p.Arg427Pro
XM_011541870.2:c.1280G>C	XP_011540172.1:p.Arg427Pro
NM_001195010.2:c.1421G>C	NP_001181939.1:p.Arg474Pro
NM_198173.3:c.1559G>C MANE Select	NP_937816.1:p.Arg520Pro
NM_198174.3:c.1559G>C	NP_937817.3:p.Arg520Pro
NM_021180.4:c.1574G>C	NP_067003.2:p.Arg525Pro