Canonical Allele Identifier: CA2680958583

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158146744-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146744A>G , CM000668.2:g.158146744A>G	GRCh38
NC_000006.11:g.158567776A>G , CM000668.1:g.158567776A>G	GRCh37
NC_000006.10:g.158487764A>G	NCBI36
NG_032889.1:g.26537T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*321+38T>C	ENSP00000475855.1:n.*321+38T>C
ENST00000642244.1:c.397+38T>C	ENSP00000493554.1:n.397+38T>C
ENST00000642903.1:c.487+38T>C	ENSP00000493559.1:n.487+38T>C
ENST00000644972.1:c.487+38T>C	ENSP00000496451.1:n.487+38T>C
ENST00000645077.1:c.*321+38T>C	ENSP00000496113.1:n.*321+38T>C
ENST00000645172.1:c.*189+2121T>C	ENSP00000495367.1:n.*189+2121T>C
ENST00000646190.1:n.1718+38T>C
ENST00000646208.1:c.223+38T>C	ENSP00000493723.1:n.223+38T>C
ENST00000646410.1:c.358+38T>C	ENSP00000494205.1:n.358+38T>C
ENST00000646562.1:c.*321+38T>C	ENSP00000496087.1:n.*321+38T>C
ENST00000647468.2:c.487+38T>C MANE Select	ENSP00000496731.1:n.487+38T>C
ENST00000648111.1:c.*131+38T>C	ENSP00000497275.1:n.*131+38T>C
ENST00000367101.5:c.487+38T>C	ENSP00000356068.1:n.487+38T>C
ENST00000367104.7:c.487+38T>C	ENSP00000356071.3:n.487+38T>C
ENST00000606965.5:c.487+38T>C	ENSP00000475808.1:n.487+38T>C
ENST00000607000.1:c.*21T>C	ENSP00000475788.1:n.*21T>C
ENST00000607071.5:c.*321+38T>C	ENSP00000475855.1:n.*321+38T>C
ENST00000607742.5:c.*321+38T>C	ENSP00000475523.1:n.*321+38T>C
NM_032861.3:c.487+38T>C	NP_116250.3:n.487+38T>C
NR_073096.1:n.629+38T>C
XM_006715586.1:c.277+38T>C	XP_006715649.1:n.277+38T>C
XM_011536196.1:c.466+38T>C	XP_011534498.1:n.466+38T>C
XM_011536197.1:c.487+38T>C	XP_011534499.1:n.487+38T>C
XM_011536198.1:c.277+38T>C	XP_011534500.1:n.277+38T>C
XR_942606.1:n.488+38T>C
XM_006715586.3:c.277+38T>C	XP_006715649.1:n.277+38T>C
XM_011536196.3:c.466+38T>C	XP_011534498.1:n.466+38T>C
XM_011536198.3:c.277+38T>C	XP_011534500.1:n.277+38T>C
XM_024446573.1:c.487+38T>C	XP_024302341.1:n.487+38T>C
XR_001743697.2:n.568+38T>C
XR_942606.2:n.619+38T>C
NM_032861.4:c.487+38T>C MANE Select	NP_116250.3:n.487+38T>C
NR_073096.2:n.611+38T>C