Canonical Allele Identifier: CA413309442
Gene: AMER1 HGNC NCBI

Linked Data

gnomAD v4: X-64192476-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192476G>T , CM000685.2:g.64192476G>T GRCh38
NC_000023.10:g.63412356G>T , CM000685.1:g.63412356G>T GRCh37
NC_000023.9:g.63329081G>T NCBI36
NG_021345.1:g.18269C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.811C>A MANE Select ENSP00000364003.4:p.Gln271Lys
ENST00000330258.3:c.811C>A ENSP00000329117.3:p.Gln271Lys
ENST00000374869.7:c.811C>A ENSP00000364003.3:p.Gln271Lys
NM_152424.3:c.811C>A NP_689637.3:p.Gln271Lys
XM_011530858.1:c.811C>A XP_011529160.1:p.Gln271Lys
NM_152424.4:c.811C>A MANE Select NP_689637.3:p.Gln271Lys