Canonical Allele Identifier: CA366264629

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158146830-T-C
• MyVariant Identifiers: chr6:g.158567862T>C (hg19) ; chr6:g.158146830T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146830T>C , CM000668.2:g.158146830T>C	GRCh38
NC_000006.11:g.158567862T>C , CM000668.1:g.158567862T>C	GRCh37
NC_000006.10:g.158487850T>C	NCBI36
NG_032889.1:g.26451A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*273A>G	ENSP00000475855.1:n.*273A>G
ENST00000642244.1:c.349A>G	ENSP00000493554.1:p.Thr117Ala
ENST00000642903.1:c.439A>G	ENSP00000493559.1:p.Thr147Ala
ENST00000644972.1:c.439A>G	ENSP00000496451.1:p.Thr147Ala
ENST00000645077.1:c.*273A>G	ENSP00000496113.1:n.*273A>G
ENST00000645172.1:c.*189+2035A>G	ENSP00000495367.1:n.*189+2035A>G
ENST00000646190.1:n.1670A>G
ENST00000646208.1:c.175A>G	ENSP00000493723.1:p.Thr59Ala
ENST00000646410.1:c.310A>G	ENSP00000494205.1:p.Thr104Ala
ENST00000646562.1:c.*273A>G	ENSP00000496087.1:n.*273A>G
ENST00000647468.2:c.439A>G MANE Select	ENSP00000496731.1:p.Thr147Ala
ENST00000648111.1:c.*83A>G	ENSP00000497275.1:n.*83A>G
ENST00000367101.5:c.439A>G	ENSP00000356068.1:p.Thr147Ala
ENST00000367104.7:c.439A>G	ENSP00000356071.3:p.Thr147Ala
ENST00000606965.5:c.439A>G	ENSP00000475808.1:p.Thr147Ala
ENST00000607000.1:c.439A>G	ENSP00000475788.1:p.Thr147Ala
ENST00000607071.5:c.*273A>G	ENSP00000475855.1:n.*273A>G
ENST00000607742.5:c.*273A>G	ENSP00000475523.1:n.*273A>G
NM_032861.3:c.439A>G	NP_116250.3:p.Thr147Ala
NR_073096.1:n.581A>G
XM_006715586.1:c.229A>G	XP_006715649.1:p.Thr77Ala
XM_011536196.1:c.418A>G	XP_011534498.1:p.Thr140Ala
XM_011536197.1:c.439A>G	XP_011534499.1:p.Thr147Ala
XM_011536198.1:c.229A>G	XP_011534500.1:p.Thr77Ala
XR_942606.1:n.440A>G
XM_006715586.3:c.229A>G	XP_006715649.1:p.Thr77Ala
XM_011536196.3:c.418A>G	XP_011534498.1:p.Thr140Ala
XM_011536198.3:c.229A>G	XP_011534500.1:p.Thr77Ala
XM_024446573.1:c.439A>G	XP_024302341.1:p.Thr147Ala
XR_001743697.2:n.520A>G
XR_942606.2:n.571A>G
NM_032861.4:c.439A>G MANE Select	NP_116250.3:p.Thr147Ala
NR_073096.2:n.563A>G