Canonical Allele Identifier: CA413308168
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs2147088785

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192047G>C , CM000685.2:g.64192047G>C GRCh38
NC_000023.10:g.63411927G>C , CM000685.1:g.63411927G>C GRCh37
NC_000023.9:g.63328652G>C NCBI36
NG_021345.1:g.18698C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.1240C>G MANE Select ENSP00000364003.4:p.Gln414Glu
ENST00000330258.3:c.1240C>G ENSP00000329117.3:p.Gln414Glu
ENST00000374869.7:c.1240C>G ENSP00000364003.3:p.Gln414Glu
NM_152424.3:c.1240C>G NP_689637.3:p.Gln414Glu
XM_011530858.1:c.1240C>G XP_011529160.1:p.Gln414Glu
NM_152424.4:c.1240C>G MANE Select NP_689637.3:p.Gln414Glu