Canonical Allele Identifier: CA1057368988

Gene: NMRAL2P

Linked Data

• dbSNP Id: rs1744965380
• gnomAD v3: 3-185969015-G-GT
• gnomAD v4: 3-185969015-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185969015_185969016insT , CM000665.2:g.185969015_185969016insT	GRCh38
NC_000003.11:g.185686804_185686805insT , CM000665.1:g.185686804_185686805insT	GRCh37
NC_000003.10:g.187169498_187169499insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306399.3:n.270+307_270+308insT
ENST00000416764.5:n.349+298_349+299insT
ENST00000422108.5:n.288+366_288+367insT
ENST00000423298.5:n.137-2600_137-2599insT
ENST00000436375.5:n.342+307_342+308insT
ENST00000445507.1:n.279+366_279+367insT
NR_033752.2:n.349+298_349+299insT
NR_151491.1:n.137-2600_137-2599insT