Canonical Allele Identifier: CA487995757

Gene: AMN

Linked Data

• dbSNP Id: rs1891080798
• gnomAD v4: 14-102922665-T-TC
• MyVariant Identifiers: chr14:g.103389002_103389003insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922665_102922666insC , CM000676.2:g.102922665_102922666insC	GRCh38
NC_000014.8:g.103389002_103389003insC , CM000676.1:g.103389002_103389003insC	GRCh37
NC_000014.7:g.102458755_102458756insC	NCBI36
NG_008276.2:g.5010_5011insC , LRG_642:g.5010_5011insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.-24_-23insC MANE Select	ENSP00000299155.6:n.-24_-23insC
ENST00000299155.9:c.-24_-23insC	ENSP00000299155.5:n.-24_-23insC
NM_030943.3:c.-24_-23insC , LRG_642t1:c.-24_-23insC	NP_112205.2:n.-24_-23insC
XM_011537202.1:c.-205_-204insC	XP_011535504.1:n.-205_-204insC
XM_011537202.3:c.-205_-204insC	XP_011535504.1:n.-205_-204insC
XM_024449714.1:c.73_74insC	XP_024305482.1:p.Trp25SerfsTer?
NM_030943.4:c.-24_-23insC MANE Select	NP_112205.2:n.-24_-23insC