Canonical Allele Identifier: CA156710
Community Standard Title: NM_152424.4(AMER1):c.477T>G (p.Phe159Leu)
Gene: AMER1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192810A>C , CM000685.2:g.64192810A>C GRCh38
NC_000023.10:g.63412690A>C , CM000685.1:g.63412690A>C GRCh37
NC_000023.9:g.63329415A>C NCBI36
NG_021345.1:g.17935T>G

Transcript Alleles

HGVS Amino-acid Change
NM_152424.4:c.477T>G MANE Select NP_689637.3:p.Phe159Leu
ENST00000374869.8:c.477T>G MANE Select ENSP00000364003.4:p.Phe159Leu
NM_152424.3:c.477T>G NP_689637.3:p.Phe159Leu
ENST00000330258.3:c.477T>G ENSP00000329117.3:p.Phe159Leu
ENST00000374869.7:c.477T>G ENSP00000364003.3:p.Phe159Leu
XM_011530858.1:c.477T>G XP_011529160.1:p.Phe159Leu