Canonical Allele Identifier: CA1453073731
Gene: GRXCR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962899_42962908delinsCAACTGATCT , CM000666.2:g.42962899_42962908delinsCAACTGATCT GRCh38
NC_000004.11:g.42964916_42964925delinsCAACTGATCT , CM000666.1:g.42964916_42964925delinsCAACTGATCT GRCh37
NC_000004.10:g.42659673_42659682delinsCAACTGATCT NCBI36
NG_027718.1:g.74634_74643delinsCAACTGATCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.392_401delinsCAACTGATCT MANE Select ENSP00000382670.2:p.Ser131=
ENST00000399770.2:c.392_401delinsCAACTGATCT ENSP00000382670.2:p.Ser131=
NM_001080476.2:c.392_401delinsCAACTGATCT NP_001073945.1:p.Ser131=
XM_011513691.1:c.29_38delinsCAACTGATCT XP_011511993.1:p.Ser10=
NM_001080476.3:c.392_401delinsCAACTGATCT MANE Select NP_001073945.1:p.Ser131=