Canonical Allele Identifier: CA366265063
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158146913T>C , CM000668.2:g.158146913T>C GRCh38
NC_000006.11:g.158567945T>C , CM000668.1:g.158567945T>C GRCh37
NC_000006.10:g.158487933T>C NCBI36
NG_032889.1:g.26368A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*190A>G ENSP00000475855.1:n.*190A>G
ENST00000642244.1:c.266A>G ENSP00000493554.1:p.Asp89Gly
ENST00000642903.1:c.356A>G ENSP00000493559.1:p.Asp119Gly
ENST00000643093.1:n.406A>G
ENST00000644972.1:c.356A>G ENSP00000496451.1:p.Asp119Gly
ENST00000645077.1:c.*190A>G ENSP00000496113.1:n.*190A>G
ENST00000645172.1:c.*189+1952A>G ENSP00000495367.1:n.*189+1952A>G
ENST00000646190.1:n.1587A>G
ENST00000646208.1:c.92A>G ENSP00000493723.1:p.Asn31Ser
ENST00000646410.1:c.227A>G ENSP00000494205.1:p.Asp76Gly
ENST00000646562.1:c.*190A>G ENSP00000496087.1:n.*190A>G
ENST00000647468.2:c.356A>G MANE Select ENSP00000496731.1:p.Asp119Gly
ENST00000648111.1:c.330A>G ENSP00000497275.1:p.Ter110Trp
ENST00000367101.5:c.356A>G ENSP00000356068.1:p.Asp119Gly
ENST00000367104.7:c.356A>G ENSP00000356071.3:p.Asp119Gly
ENST00000606965.5:c.356A>G ENSP00000475808.1:p.Asp119Gly
ENST00000607000.1:c.356A>G ENSP00000475788.1:p.Asp119Gly
ENST00000607071.5:c.*190A>G ENSP00000475855.1:n.*190A>G
ENST00000607742.5:c.*190A>G ENSP00000475523.1:n.*190A>G
NM_032861.3:c.356A>G NP_116250.3:p.Asp119Gly
NR_073096.1:n.498A>G
XM_006715586.1:c.146A>G XP_006715649.1:p.Asp49Gly
XM_011536196.1:c.335A>G XP_011534498.1:p.Asp112Gly
XM_011536197.1:c.356A>G XP_011534499.1:p.Asp119Gly
XM_011536198.1:c.146A>G XP_011534500.1:p.Asp49Gly
XR_942606.1:n.357A>G
XM_006715586.3:c.146A>G XP_006715649.1:p.Asp49Gly
XM_011536196.3:c.335A>G XP_011534498.1:p.Asp112Gly
XM_011536198.3:c.146A>G XP_011534500.1:p.Asp49Gly
XM_024446573.1:c.356A>G XP_024302341.1:p.Asp119Gly
XR_001743697.2:n.437A>G
XR_942606.2:n.488A>G
NM_032861.4:c.356A>G MANE Select NP_116250.3:p.Asp119Gly
NR_073096.2:n.480A>G