Canonical Allele Identifier: CA366265075

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158146915-T-C
• MyVariant Identifiers: chr6:g.158567947T>C (hg19) ; chr6:g.158146915T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146915T>C , CM000668.2:g.158146915T>C	GRCh38
NC_000006.11:g.158567947T>C , CM000668.1:g.158567947T>C	GRCh37
NC_000006.10:g.158487935T>C	NCBI36
NG_032889.1:g.26366A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*190-2A>G	ENSP00000475855.1:n.*190-2A>G
ENST00000642244.1:c.266-2A>G	ENSP00000493554.1:n.266-2A>G
ENST00000642903.1:c.356-2A>G	ENSP00000493559.1:n.356-2A>G
ENST00000643093.1:n.406-2A>G
ENST00000644972.1:c.356-2A>G	ENSP00000496451.1:n.356-2A>G
ENST00000645077.1:c.*190-2A>G	ENSP00000496113.1:n.*190-2A>G
ENST00000645172.1:c.*189+1950A>G	ENSP00000495367.1:n.*189+1950A>G
ENST00000646190.1:n.1587-2A>G
ENST00000646208.1:c.92-2A>G	ENSP00000493723.1:n.92-2A>G
ENST00000646410.1:c.227-2A>G	ENSP00000494205.1:n.227-2A>G
ENST00000646562.1:c.*190-2A>G	ENSP00000496087.1:n.*190-2A>G
ENST00000647468.2:c.356-2A>G MANE Select	ENSP00000496731.1:n.356-2A>G
ENST00000648111.1:c.330-2A>G	ENSP00000497275.1:n.330-2A>G
ENST00000367101.5:c.356-2A>G	ENSP00000356068.1:n.356-2A>G
ENST00000367104.7:c.356-2A>G	ENSP00000356071.3:n.356-2A>G
ENST00000606965.5:c.356-2A>G	ENSP00000475808.1:n.356-2A>G
ENST00000607000.1:c.356-2A>G	ENSP00000475788.1:n.356-2A>G
ENST00000607071.5:c.*190-2A>G	ENSP00000475855.1:n.*190-2A>G
ENST00000607742.5:c.*190-2A>G	ENSP00000475523.1:n.*190-2A>G
NM_032861.3:c.356-2A>G	NP_116250.3:n.356-2A>G
NR_073096.1:n.498-2A>G
XM_006715586.1:c.146-2A>G	XP_006715649.1:n.146-2A>G
XM_011536196.1:c.335-2A>G	XP_011534498.1:n.335-2A>G
XM_011536197.1:c.356-2A>G	XP_011534499.1:n.356-2A>G
XM_011536198.1:c.146-2A>G	XP_011534500.1:n.146-2A>G
XR_942606.1:n.357-2A>G
XM_006715586.3:c.146-2A>G	XP_006715649.1:n.146-2A>G
XM_011536196.3:c.335-2A>G	XP_011534498.1:n.335-2A>G
XM_011536198.3:c.146-2A>G	XP_011534500.1:n.146-2A>G
XM_024446573.1:c.356-2A>G	XP_024302341.1:n.356-2A>G
XR_001743697.2:n.437-2A>G
XR_942606.2:n.488-2A>G
NM_032861.4:c.356-2A>G MANE Select	NP_116250.3:n.356-2A>G
NR_073096.2:n.480-2A>G