Canonical Allele Identifier: CA391078925

Gene: AMN

Linked Data

• gnomAD v4: 14-102922699-T-C
• MyVariant Identifiers: chr14:g.103389036T>C (hg19) ; chr14:g.102922699T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102922699T>C , CM000676.2:g.102922699T>C	GRCh38
NC_000014.8:g.103389036T>C , CM000676.1:g.103389036T>C	GRCh37
NC_000014.7:g.102458789T>C	NCBI36
NG_008276.2:g.5044T>C , LRG_642:g.5044T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299155.10:c.11T>C MANE Select	ENSP00000299155.6:p.Leu4Pro
ENST00000299155.9:c.11T>C	ENSP00000299155.5:p.Leu4Pro
NM_030943.3:c.11T>C , LRG_642t1:c.11T>C	NP_112205.2:p.Leu4Pro
XM_011537202.1:c.-171T>C	XP_011535504.1:n.-171T>C
XM_011537202.3:c.-171T>C	XP_011535504.1:n.-171T>C
XM_024449714.1:c.107T>C	XP_024305482.1:p.Leu36Pro
NM_030943.4:c.11T>C MANE Select	NP_112205.2:p.Leu4Pro