Canonical Allele Identifier: CA7359661

Gene: AMN

Linked Data

• dbSNP Id: rs772396092
• ExAC: 14:103388996 TC / T
• gnomAD v2: 14-103388996-TC-T
• gnomAD v3: 14-102922659-TC-T
• gnomAD v4: 14-102922659-TC-T
• MyVariant Identifiers: chr14:g.103388997del (hg19) ; chr14:g.102922660del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922661del , CM000676.2:g.102922661del	GRCh38
NC_000014.8:g.103388998del , CM000676.1:g.103388998del	GRCh37
NC_000014.7:g.102458751del	NCBI36
NG_008276.2:g.5006del , LRG_642:g.5006del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.9:c.-28del	ENSP00000299155.5:n.-28del
NM_030943.3:c.-28del , LRG_642t1:c.-28del	NP_112205.2:n.-28del
XM_011537202.1:c.-209del	XP_011535504.1:n.-209del
XM_011537202.3:c.-209del	XP_011535504.1:n.-209del
XM_024449714.1:c.69del	XP_024305482.1:p.Trp24GlyfsTer25