Canonical Allele Identifier: CA371644204
Community Standard Title: NM_024915.4(GRHL2):c.548G>C (p.Arg183Pro)
Gene: GRHL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101558682G>C , CM000670.2:g.101558682G>C GRCh38
NC_000008.10:g.102570910G>C , CM000670.1:g.102570910G>C GRCh37
NC_000008.9:g.102640086G>C NCBI36
NG_011971.1:g.71243G>C
NG_011971.2:g.71243G>C

Transcript Alleles

HGVS Amino-acid Change
NM_024915.4:c.548G>C MANE Select NP_079191.2:p.Arg183Pro
ENST00000646743.1:c.548G>C MANE Select ENSP00000495564.1:p.Arg183Pro
NM_001330593.1:c.500G>C NP_001317522.1:p.Arg167Pro
NM_001330593.2:c.500G>C NP_001317522.1:p.Arg167Pro
NM_024915.3:c.548G>C NP_079191.2:p.Arg183Pro
ENST00000251808.7:c.548G>C ENSP00000251808.3:p.Arg183Pro
ENST00000395927.1:c.500G>C ENSP00000379260.1:p.Arg167Pro
XM_011517305.1:c.500G>C XP_011515607.1:p.Arg167Pro
XM_011517306.1:c.500G>C XP_011515608.1:p.Arg167Pro
XM_011517306.3:c.500G>C XP_011515608.1:p.Arg167Pro
XM_011517307.1:c.548G>C XP_011515609.1:p.Arg183Pro
XM_011517307.3:c.548G>C XP_011515609.1:p.Arg183Pro