Canonical Allele Identifier: CA347267329
Community Standard Title: NM_001378454.1(ALMS1):c.2231C>G (p.Ser744Ter)
Gene: ALMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73448758C>G , CM000664.2:g.73448758C>G GRCh38
NC_000002.11:g.73675885C>G , CM000664.1:g.73675885C>G GRCh37
NC_000002.10:g.73529393C>G NCBI36
NG_011690.1:g.68006C>G , LRG_741:g.68006C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378454.1:c.2231C>G MANE Select NP_001365383.1:p.Ser744Ter
ENST00000613296.6:c.2231C>G MANE Select ENSP00000482968.1:p.Ser744Ter
NM_015120.4:c.2234C>G , LRG_741t1:c.2234C>G NP_055935.4:p.Ser745Ter
ENST00000484298.5:c.2105C>G ENSP00000478155.1:p.Ser702Ter
ENST00000613296.4:c.2231C>G ENSP00000482968.1:p.Ser744Ter
ENST00000614410.4:c.2231C>G ENSP00000479094.1:p.Ser744Ter
ENST00000682565.1:c.1850C>G ENSP00000507671.1:p.Ser617Ter
ENST00000682801.1:c.1850C>G ENSP00000507862.1:p.Ser617Ter
ENST00000682859.1:c.1850C>G ENSP00000508222.1:p.Ser617Ter
ENST00000683791.1:c.685+16467C>G
ENST00000684548.1:c.1850C>G ENSP00000507421.1:p.Ser617Ter