Canonical Allele Identifier: CA2626672700
Gene: AMN HGNC NCBI

Linked Data

gnomAD v4: 14-102922791-C-CTA
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102922791_102922792insTA , CM000676.2:g.102922791_102922792insTA GRCh38
NC_000014.8:g.103389128_103389129insTA , CM000676.1:g.103389128_103389129insTA GRCh37
NC_000014.7:g.102458881_102458882insTA NCBI36
NG_008276.2:g.5136_5137insTA , LRG_642:g.5136_5137insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299155.10:c.43+60_43+61insTA MANE Select ENSP00000299155.6:n.43+60_43+61insTA
ENST00000299155.9:c.43+60_43+61insTA ENSP00000299155.5:n.43+60_43+61insTA
NM_030943.3:c.43+60_43+61insTA , LRG_642t1:c.43+60_43+61insTA NP_112205.2:n.43+60_43+61insTA
XM_011537202.1:c.-120+41_-120+42insTA XP_011535504.1:n.-120+41_-120+42insTA
XM_011537202.3:c.-120+41_-120+42insTA XP_011535504.1:n.-120+41_-120+42insTA
XM_024449714.1:c.139+60_139+61insTA XP_024305482.1:n.139+60_139+61insTA
NM_030943.4:c.43+60_43+61insTA MANE Select NP_112205.2:n.43+60_43+61insTA
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