Canonical Allele Identifier: CA2952100
Gene: ENAM HGNC NCBI

Linked Data

dbSNP Id: rs747332622
gnomAD v2: 4-71508411-A-G
gnomAD v3: 4-70642694-A-G
gnomAD v4: 4-70642694-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642694A>G , CM000666.2:g.70642694A>G GRCh38
NC_000004.11:g.71508411A>G , CM000666.1:g.71508411A>G GRCh37
NC_000004.10:g.71727275A>G NCBI36
NG_013024.1:g.18951A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1268A>G MANE Select ENSP00000379383.4:p.Lys423Arg
ENST00000396073.3:c.1268A>G ENSP00000379383.3:p.Lys423Arg
ENST00000472903.5:n.99+4851A>G
NM_031889.2:c.1268A>G NP_114095.2:p.Lys423Arg
XM_006714056.2:c.1268A>G XP_006714119.1:p.Lys423Arg
XM_006714056.4:c.1268A>G XP_006714119.1:p.Lys423Arg
NM_001368133.1:c.614A>G NP_001355062.1:p.Lys205Arg
NM_031889.3:c.1268A>G MANE Select NP_114095.2:p.Lys423Arg