Canonical Allele Identifier: CA366255020

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114854-G-C
• MyVariant Identifiers: chr6:g.158535886G>C (hg19) ; chr6:g.158114854G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114854G>C , CM000668.2:g.158114854G>C	GRCh38
NC_000006.11:g.158535886G>C , CM000668.1:g.158535886G>C	GRCh37
NC_000006.10:g.158455874G>C	NCBI36
NG_032889.1:g.58427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.831C>G	ENSP00000391168.2:n.831C>G
ENST00000607071.6:c.*1339C>G	ENSP00000475855.1:n.*1339C>G
ENST00000642244.1:c.1529C>G	ENSP00000493554.1:p.Ala510Gly
ENST00000642903.1:c.1619C>G	ENSP00000493559.1:p.Ala540Gly
ENST00000644972.1:c.1619C>G	ENSP00000496451.1:p.Ala540Gly
ENST00000645077.1:c.*1240C>G	ENSP00000496113.1:n.*1240C>G
ENST00000645172.1:c.*1321C>G	ENSP00000495367.1:n.*1321C>G
ENST00000646190.1:n.2950C>G
ENST00000646208.1:c.1355C>G	ENSP00000493723.1:p.Ala452Gly
ENST00000646410.1:c.1490C>G	ENSP00000494205.1:p.Ala497Gly
ENST00000646562.1:c.*1453C>G	ENSP00000496087.1:n.*1453C>G
ENST00000647468.2:c.1619C>G MANE Select	ENSP00000496731.1:p.Ala540Gly
ENST00000648111.1:c.*1307C>G	ENSP00000497275.1:n.*1307C>G
ENST00000367101.5:c.*67C>G	ENSP00000356068.1:n.*67C>G
ENST00000367104.7:c.1619C>G	ENSP00000356071.3:p.Ala540Gly
ENST00000435180.5:c.344C>G	ENSP00000391168.1:p.Ala115Gly
ENST00000606965.5:c.*180C>G	ENSP00000475808.1:n.*180C>G
ENST00000607071.5:c.*1553C>G	ENSP00000475855.1:n.*1553C>G
ENST00000607742.5:c.*2897C>G	ENSP00000475523.1:n.*2897C>G
NM_032861.3:c.1619C>G	NP_116250.3:p.Ala540Gly
NR_073096.1:n.1552C>G
XM_006715586.1:c.1409C>G	XP_006715649.1:p.Ala470Gly
XM_011536196.1:c.1598C>G	XP_011534498.1:p.Ala533Gly
XM_011536197.1:c.1505C>G	XP_011534499.1:p.Ala502Gly
XM_011536198.1:c.1409C>G	XP_011534500.1:p.Ala470Gly
XM_006715586.3:c.1409C>G	XP_006715649.1:p.Ala470Gly
XM_011536196.3:c.1598C>G	XP_011534498.1:p.Ala533Gly
XM_011536198.3:c.1409C>G	XP_011534500.1:p.Ala470Gly
XM_024446573.1:c.1619C>G	XP_024302341.1:p.Ala540Gly
XR_001743697.2:n.1650C>G
XR_942606.2:n.1701C>G
NM_032861.4:c.1619C>G MANE Select	NP_116250.3:p.Ala540Gly
NR_073096.2:n.1534C>G