Canonical Allele Identifier: CA2680956766

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114840-T-TAACA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114841_158114844dup , CM000668.2:g.158114841_158114844dup	GRCh38
NC_000006.11:g.158535873_158535876dup , CM000668.1:g.158535873_158535876dup	GRCh37
NC_000006.10:g.158455861_158455864dup	NCBI36
NG_032889.1:g.58437_58440dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.841_844dup	ENSP00000391168.2:n.841_844dup
ENST00000607071.6:c.*1349_*1352dup	ENSP00000475855.1:n.*1349_*1352dup
ENST00000642244.1:c.1539_1542dup	ENSP00000493554.1:p.Asn515CysfsTer2
ENST00000642903.1:c.1629_1632dup	ENSP00000493559.1:p.Asn545CysfsTer2
ENST00000644972.1:c.1629_1632dup	ENSP00000496451.1:p.Asn545CysfsTer2
ENST00000645077.1:c.*1250_*1253dup	ENSP00000496113.1:n.*1250_*1253dup
ENST00000645172.1:c.*1331_*1334dup	ENSP00000495367.1:n.*1331_*1334dup
ENST00000646190.1:n.2960_2963dup
ENST00000646208.1:c.1365_1368dup	ENSP00000493723.1:p.Asn457CysfsTer2
ENST00000646410.1:c.1500_1503dup	ENSP00000494205.1:p.Asn502CysfsTer2
ENST00000646562.1:c.*1463_*1466dup	ENSP00000496087.1:n.*1463_*1466dup
ENST00000647468.2:c.1629_1632dup MANE Select	ENSP00000496731.1:p.Asn545CysfsTer2
ENST00000648111.1:c.*1317_*1320dup	ENSP00000497275.1:n.*1317_*1320dup
ENST00000367101.5:c.*77_*80dup	ENSP00000356068.1:n.*77_*80dup
ENST00000367104.7:c.1629_1632dup	ENSP00000356071.3:p.Asn545CysfsTer2
ENST00000435180.5:c.354_357dup	ENSP00000391168.1:p.Asn120CysfsTer2
ENST00000606965.5:c.*190_*193dup	ENSP00000475808.1:n.*190_*193dup
ENST00000607071.5:c.*1563_*1566dup	ENSP00000475855.1:n.*1563_*1566dup
ENST00000607742.5:c.*2907_*2910dup	ENSP00000475523.1:n.*2907_*2910dup
NM_032861.3:c.1629_1632dup	NP_116250.3:p.Asn545CysfsTer2
NR_073096.1:n.1562_1565dup
XM_006715586.1:c.1419_1422dup	XP_006715649.1:p.Asn475CysfsTer2
XM_011536196.1:c.1608_1611dup	XP_011534498.1:p.Asn538CysfsTer2
XM_011536197.1:c.1515_1518dup	XP_011534499.1:p.Asn507CysfsTer2
XM_011536198.1:c.1419_1422dup	XP_011534500.1:p.Asn475CysfsTer2
XM_006715586.3:c.1419_1422dup	XP_006715649.1:p.Asn475CysfsTer2
XM_011536196.3:c.1608_1611dup	XP_011534498.1:p.Asn538CysfsTer2
XM_011536198.3:c.1419_1422dup	XP_011534500.1:p.Asn475CysfsTer2
XM_024446573.1:c.1629_1632dup	XP_024302341.1:p.Asn545CysfsTer2
XR_001743697.2:n.1660_1663dup
XR_942606.2:n.1711_1714dup
NM_032861.4:c.1629_1632dup MANE Select	NP_116250.3:p.Asn545CysfsTer2
NR_073096.2:n.1544_1547dup