Canonical Allele Identifier: CA366254876

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114788-C-G
• MyVariant Identifiers: chr6:g.158535820C>G (hg19) ; chr6:g.158114788C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114788C>G , CM000668.2:g.158114788C>G	GRCh38
NC_000006.11:g.158535820C>G , CM000668.1:g.158535820C>G	GRCh37
NC_000006.10:g.158455808C>G	NCBI36
NG_032889.1:g.58493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+1G>C	ENSP00000475855.1:n.*1404+1G>C
ENST00000642244.1:c.1594+1G>C	ENSP00000493554.1:n.1594+1G>C
ENST00000642903.1:c.1685G>C	ENSP00000493559.1:p.Gly562Ala
ENST00000644972.1:c.1684+1G>C	ENSP00000496451.1:n.1684+1G>C
ENST00000645077.1:c.*1305+1G>C	ENSP00000496113.1:n.*1305+1G>C
ENST00000645172.1:c.*1386+1G>C	ENSP00000495367.1:n.*1386+1G>C
ENST00000646190.1:n.3015+1G>C
ENST00000646208.1:c.1420+1G>C	ENSP00000493723.1:n.1420+1G>C
ENST00000646410.1:c.1555+1G>C	ENSP00000494205.1:n.1555+1G>C
ENST00000646562.1:c.*1519G>C	ENSP00000496087.1:n.*1519G>C
ENST00000647468.2:c.1684+1G>C MANE Select	ENSP00000496731.1:n.1684+1G>C
ENST00000648111.1:c.*1372+1G>C	ENSP00000497275.1:n.*1372+1G>C
ENST00000367101.5:c.*133G>C	ENSP00000356068.1:n.*133G>C
ENST00000367104.7:c.1684+1G>C	ENSP00000356071.3:n.1684+1G>C
ENST00000435180.5:c.410G>C	ENSP00000391168.1:p.Gly137Ala
ENST00000606965.5:c.*246G>C	ENSP00000475808.1:n.*246G>C
ENST00000607071.5:c.*1618+1G>C	ENSP00000475855.1:n.*1618+1G>C
ENST00000607742.5:c.*2962+1G>C	ENSP00000475523.1:n.*2962+1G>C
NM_032861.3:c.1684+1G>C	NP_116250.3:n.1684+1G>C
NR_073096.1:n.1618G>C
XM_006715586.1:c.1474+1G>C	XP_006715649.1:n.1474+1G>C
XM_011536196.1:c.1663+1G>C	XP_011534498.1:n.1663+1G>C
XM_011536197.1:c.1570+1G>C	XP_011534499.1:n.1570+1G>C
XM_011536198.1:c.1474+1G>C	XP_011534500.1:n.1474+1G>C
XM_006715586.3:c.1474+1G>C	XP_006715649.1:n.1474+1G>C
XM_011536196.3:c.1663+1G>C	XP_011534498.1:n.1663+1G>C
XM_011536198.3:c.1474+1G>C	XP_011534500.1:n.1474+1G>C
XM_024446573.1:c.1684+1G>C	XP_024302341.1:n.1684+1G>C
XR_001743697.2:n.1715+1G>C
XR_942606.2:n.1766+1G>C
NM_032861.4:c.1684+1G>C MANE Select	NP_116250.3:n.1684+1G>C
NR_073096.2:n.1600G>C