Canonical Allele Identifier: CA413308893
Gene: AMER1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192352A>G , CM000685.2:g.64192352A>G GRCh38
NC_000023.10:g.63412232A>G , CM000685.1:g.63412232A>G GRCh37
NC_000023.9:g.63328957A>G NCBI36
NG_021345.1:g.18393T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.935T>C MANE Select ENSP00000364003.4:p.Leu312Ser
ENST00000330258.3:c.935T>C ENSP00000329117.3:p.Leu312Ser
ENST00000374869.7:c.935T>C ENSP00000364003.3:p.Leu312Ser
NM_152424.3:c.935T>C NP_689637.3:p.Leu312Ser
XM_011530858.1:c.935T>C XP_011529160.1:p.Leu312Ser
NM_152424.4:c.935T>C MANE Select NP_689637.3:p.Leu312Ser