Canonical Allele Identifier: CA391078904

Gene: AMN

Linked Data

• MyVariant Identifiers: chr14:g.103389026A>T (hg19) ; chr14:g.102922689A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922689A>T , CM000676.2:g.102922689A>T	GRCh38
NC_000014.8:g.103389026A>T , CM000676.1:g.103389026A>T	GRCh37
NC_000014.7:g.102458779A>T	NCBI36
NG_008276.2:g.5034A>T , LRG_642:g.5034A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.1A>T MANE Select	ENSP00000299155.6:p.Met1Leu
ENST00000299155.9:c.1A>T	ENSP00000299155.5:p.Met1Leu
NM_030943.3:c.1A>T , LRG_642t1:c.1A>T	NP_112205.2:p.Met1Leu
XM_011537202.1:c.-181A>T	XP_011535504.1:n.-181A>T
XM_011537202.3:c.-181A>T	XP_011535504.1:n.-181A>T
XM_024449714.1:c.97A>T	XP_024305482.1:p.Met33Leu
NM_030943.4:c.1A>T MANE Select	NP_112205.2:p.Met1Leu