Canonical Allele Identifier: CA512150640
Gene: SYNJ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32727996G>C , CM000683.2:g.32727996G>C GRCh38
NC_000021.8:g.34100307G>C , CM000683.1:g.34100307G>C GRCh37
NC_000021.7:g.33022178G>C NCBI36
NG_030017.1:g.5045C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382499.7:c.45C>G ENSP00000371939.2:p.Gly15=
ENST00000433931.7:c.45C>G ENSP00000409667.2:p.Gly15=
ENST00000674308.1:c.-73C>G ENSP00000501426.1:n.-73C>G
ENST00000674351.1:c.-73C>G MANE Select ENSP00000501530.1:n.-73C>G
ENST00000382491.7:c.-73C>G ENSP00000371931.4:n.-73C>G
ENST00000382499.6:c.45C>G ENSP00000371939.2:p.Gly15=
ENST00000433931.6:c.45C>G ENSP00000409667.2:p.Gly15=
NM_003895.3:c.45C>G NP_003886.3:p.Gly15=
NM_203446.2:c.45C>G NP_982271.2:p.Gly15=
XM_017028495.2:c.45C>G XP_016883984.1:p.Gly15=
XM_017028497.2:c.45C>G XP_016883986.1:p.Gly15=
XM_017028499.2:c.45C>G XP_016883988.1:p.Gly15=
XM_017028505.2:c.45C>G XP_016883994.1:p.Gly15=
NM_203446.3:c.-73C>G MANE Select NP_982271.3:n.-73C>G