Canonical Allele Identifier: CA366264488

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158146769-G-T
• MyVariant Identifiers: chr6:g.158567801G>T (hg19) ; chr6:g.158146769G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146769G>T , CM000668.2:g.158146769G>T	GRCh38
NC_000006.11:g.158567801G>T , CM000668.1:g.158567801G>T	GRCh37
NC_000006.10:g.158487789G>T	NCBI36
NG_032889.1:g.26512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*321+13C>A	ENSP00000475855.1:n.*321+13C>A
ENST00000642244.1:c.397+13C>A	ENSP00000493554.1:n.397+13C>A
ENST00000642903.1:c.487+13C>A	ENSP00000493559.1:n.487+13C>A
ENST00000644972.1:c.487+13C>A	ENSP00000496451.1:n.487+13C>A
ENST00000645077.1:c.*321+13C>A	ENSP00000496113.1:n.*321+13C>A
ENST00000645172.1:c.*189+2096C>A	ENSP00000495367.1:n.*189+2096C>A
ENST00000646190.1:n.1718+13C>A
ENST00000646208.1:c.223+13C>A	ENSP00000493723.1:n.223+13C>A
ENST00000646410.1:c.358+13C>A	ENSP00000494205.1:n.358+13C>A
ENST00000646562.1:c.*321+13C>A	ENSP00000496087.1:n.*321+13C>A
ENST00000647468.2:c.487+13C>A MANE Select	ENSP00000496731.1:n.487+13C>A
ENST00000648111.1:c.*131+13C>A	ENSP00000497275.1:n.*131+13C>A
ENST00000367101.5:c.487+13C>A	ENSP00000356068.1:n.487+13C>A
ENST00000367104.7:c.487+13C>A	ENSP00000356071.3:n.487+13C>A
ENST00000606965.5:c.487+13C>A	ENSP00000475808.1:n.487+13C>A
ENST00000607000.1:c.500C>A	ENSP00000475788.1:p.Thr167Asn
ENST00000607071.5:c.*321+13C>A	ENSP00000475855.1:n.*321+13C>A
ENST00000607742.5:c.*321+13C>A	ENSP00000475523.1:n.*321+13C>A
NM_032861.3:c.487+13C>A	NP_116250.3:n.487+13C>A
NR_073096.1:n.629+13C>A
XM_006715586.1:c.277+13C>A	XP_006715649.1:n.277+13C>A
XM_011536196.1:c.466+13C>A	XP_011534498.1:n.466+13C>A
XM_011536197.1:c.487+13C>A	XP_011534499.1:n.487+13C>A
XM_011536198.1:c.277+13C>A	XP_011534500.1:n.277+13C>A
XR_942606.1:n.488+13C>A
XM_006715586.3:c.277+13C>A	XP_006715649.1:n.277+13C>A
XM_011536196.3:c.466+13C>A	XP_011534498.1:n.466+13C>A
XM_011536198.3:c.277+13C>A	XP_011534500.1:n.277+13C>A
XM_024446573.1:c.487+13C>A	XP_024302341.1:n.487+13C>A
XR_001743697.2:n.568+13C>A
XR_942606.2:n.619+13C>A
NM_032861.4:c.487+13C>A MANE Select	NP_116250.3:n.487+13C>A
NR_073096.2:n.611+13C>A