Canonical Allele Identifier: CA150915192

Gene: SERAC1

Linked Data

• dbSNP Id: rs950260896
• gnomAD v4: 6-158114941-G-T
• MyVariant Identifiers: chr6:g.158535973G>T (hg19) ; chr6:g.158114941G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114941G>T , CM000668.2:g.158114941G>T	GRCh38
NC_000006.11:g.158535973G>T , CM000668.1:g.158535973G>T	GRCh37
NC_000006.10:g.158455961G>T	NCBI36
NG_032889.1:g.58340C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.744C>A	ENSP00000391168.2:n.744C>A
ENST00000607071.6:c.*1252C>A	ENSP00000475855.1:n.*1252C>A
ENST00000642244.1:c.1442C>A	ENSP00000493554.1:p.Ala481Asp
ENST00000642903.1:c.1532C>A	ENSP00000493559.1:p.Ala511Asp
ENST00000644972.1:c.1532C>A	ENSP00000496451.1:p.Ala511Asp
ENST00000645077.1:c.*1153C>A	ENSP00000496113.1:n.*1153C>A
ENST00000645172.1:c.*1234C>A	ENSP00000495367.1:n.*1234C>A
ENST00000646190.1:n.2863C>A
ENST00000646208.1:c.1268C>A	ENSP00000493723.1:p.Ala423Asp
ENST00000646410.1:c.1403C>A	ENSP00000494205.1:p.Ala468Asp
ENST00000646562.1:c.*1366C>A	ENSP00000496087.1:n.*1366C>A
ENST00000647468.2:c.1532C>A MANE Select	ENSP00000496731.1:p.Ala511Asp
ENST00000648111.1:c.*1220C>A	ENSP00000497275.1:n.*1220C>A
ENST00000367101.5:c.1576C>A	ENSP00000356068.1:p.Pro526Thr
ENST00000367104.7:c.1532C>A	ENSP00000356071.3:p.Ala511Asp
ENST00000435180.5:c.257C>A	ENSP00000391168.1:p.Ala86Asp
ENST00000606965.5:c.*93C>A	ENSP00000475808.1:n.*93C>A
ENST00000607071.5:c.*1466C>A	ENSP00000475855.1:n.*1466C>A
ENST00000607742.5:c.*2810C>A	ENSP00000475523.1:n.*2810C>A
NM_032861.3:c.1532C>A	NP_116250.3:p.Ala511Asp
NR_073096.1:n.1465C>A
XM_006715586.1:c.1322C>A	XP_006715649.1:p.Ala441Asp
XM_011536196.1:c.1511C>A	XP_011534498.1:p.Ala504Asp
XM_011536197.1:c.1418C>A	XP_011534499.1:p.Ala473Asp
XM_011536198.1:c.1322C>A	XP_011534500.1:p.Ala441Asp
XM_006715586.3:c.1322C>A	XP_006715649.1:p.Ala441Asp
XM_011536196.3:c.1511C>A	XP_011534498.1:p.Ala504Asp
XM_011536198.3:c.1322C>A	XP_011534500.1:p.Ala441Asp
XM_024446573.1:c.1532C>A	XP_024302341.1:p.Ala511Asp
XR_001743697.2:n.1563C>A
XR_942606.2:n.1614C>A
NM_032861.4:c.1532C>A MANE Select	NP_116250.3:p.Ala511Asp
NR_073096.2:n.1447C>A