Canonical Allele Identifier: CA795064995
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1177607862
MyVariant Identifiers: chr4:g.42964911_42964912insC (hg19) chr4:g.42962894_42962895insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962896dup , CM000666.2:g.42962896dup GRCh38
NC_000004.11:g.42964913dup , CM000666.1:g.42964913dup GRCh37
NC_000004.10:g.42659670dup NCBI36
NG_027718.1:g.74631dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.389dup MANE Select ENSP00000382670.2:p.Ser131IlefsTer3
ENST00000399770.2:c.389dup ENSP00000382670.2:p.Ser131IlefsTer3
NM_001080476.2:c.389dup NP_001073945.1:p.Ser131IlefsTer3
XM_011513691.1:c.26dup XP_011511993.1:p.Ser10IlefsTer3
NM_001080476.3:c.389dup MANE Select NP_001073945.1:p.Ser131IlefsTer3
Search 100 bp 5'
Search 100 bp 3'