Canonical Allele Identifier: CA366255224
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114942C>T , CM000668.2:g.158114942C>T GRCh38
NC_000006.11:g.158535974C>T , CM000668.1:g.158535974C>T GRCh37
NC_000006.10:g.158455962C>T NCBI36
NG_032889.1:g.58339G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.743G>A ENSP00000391168.2:n.743G>A
ENST00000607071.6:c.*1251G>A ENSP00000475855.1:n.*1251G>A
ENST00000642244.1:c.1441G>A ENSP00000493554.1:p.Ala481Thr
ENST00000642903.1:c.1531G>A ENSP00000493559.1:p.Ala511Thr
ENST00000644972.1:c.1531G>A ENSP00000496451.1:p.Ala511Thr
ENST00000645077.1:c.*1152G>A ENSP00000496113.1:n.*1152G>A
ENST00000645172.1:c.*1233G>A ENSP00000495367.1:n.*1233G>A
ENST00000646190.1:n.2862G>A
ENST00000646208.1:c.1267G>A ENSP00000493723.1:p.Ala423Thr
ENST00000646410.1:c.1402G>A ENSP00000494205.1:p.Ala468Thr
ENST00000646562.1:c.*1365G>A ENSP00000496087.1:n.*1365G>A
ENST00000647468.2:c.1531G>A MANE Select ENSP00000496731.1:p.Ala511Thr
ENST00000648111.1:c.*1219G>A ENSP00000497275.1:n.*1219G>A
ENST00000367101.5:c.1575G>A ENSP00000356068.1:p.Lys525=
ENST00000367104.7:c.1531G>A ENSP00000356071.3:p.Ala511Thr
ENST00000435180.5:c.256G>A ENSP00000391168.1:p.Ala86Thr
ENST00000606965.5:c.*92G>A ENSP00000475808.1:n.*92G>A
ENST00000607071.5:c.*1465G>A ENSP00000475855.1:n.*1465G>A
ENST00000607742.5:c.*2809G>A ENSP00000475523.1:n.*2809G>A
NM_032861.3:c.1531G>A NP_116250.3:p.Ala511Thr
NR_073096.1:n.1464G>A
XM_006715586.1:c.1321G>A XP_006715649.1:p.Ala441Thr
XM_011536196.1:c.1510G>A XP_011534498.1:p.Ala504Thr
XM_011536197.1:c.1417G>A XP_011534499.1:p.Ala473Thr
XM_011536198.1:c.1321G>A XP_011534500.1:p.Ala441Thr
XM_006715586.3:c.1321G>A XP_006715649.1:p.Ala441Thr
XM_011536196.3:c.1510G>A XP_011534498.1:p.Ala504Thr
XM_011536198.3:c.1321G>A XP_011534500.1:p.Ala441Thr
XM_024446573.1:c.1531G>A XP_024302341.1:p.Ala511Thr
XR_001743697.2:n.1562G>A
XR_942606.2:n.1613G>A
NM_032861.4:c.1531G>A MANE Select NP_116250.3:p.Ala511Thr
NR_073096.2:n.1446G>A