Canonical Allele Identifier: CA795065018
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1361160791
MyVariant Identifiers: chr4:g.42964917_42964925del (hg19) chr4:g.42962900_42962908del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962901_42962909del , CM000666.2:g.42962901_42962909del GRCh38
NC_000004.11:g.42964918_42964926del , CM000666.1:g.42964918_42964926del GRCh37
NC_000004.10:g.42659675_42659683del NCBI36
NG_027718.1:g.74636_74644del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.394_402del MANE Select ENSP00000382670.2:p.Thr132_Leu134del
ENST00000399770.2:c.394_402del ENSP00000382670.2:p.Thr132_Leu134del
NM_001080476.2:c.394_402del NP_001073945.1:p.Thr132_Leu134del
XM_011513691.1:c.31_39del XP_011511993.1:p.Thr11_Leu13del
NM_001080476.3:c.394_402del MANE Select NP_001073945.1:p.Thr132_Leu134del
Search 100 bp 5'
Search 100 bp 3'