Canonical Allele Identifier: CA1675978237

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146763_158146764delinsGT , CM000668.2:g.158146763_158146764delinsGT	GRCh38
NC_000006.11:g.158567795_158567796delinsGT , CM000668.1:g.158567795_158567796delinsGT	GRCh37
NC_000006.10:g.158487783_158487784delinsGT	NCBI36
NG_032889.1:g.26517_26518delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*321+18_*321+19delinsAC	ENSP00000475855.1:n.*321+18_*321+19delinsAC
ENST00000642244.1:c.397+18_397+19delinsAC	ENSP00000493554.1:n.397+18_397+19delinsAC
ENST00000642903.1:c.487+18_487+19delinsAC	ENSP00000493559.1:n.487+18_487+19delinsAC
ENST00000644972.1:c.487+18_487+19delinsAC	ENSP00000496451.1:n.487+18_487+19delinsAC
ENST00000645077.1:c.*321+18_*321+19delinsAC	ENSP00000496113.1:n.*321+18_*321+19delinsAC
ENST00000645172.1:c.*189+2101_*189+2102delinsAC	ENSP00000495367.1:n.*189+2101_*189+2102delinsAC
ENST00000646190.1:n.1718+18_1718+19delinsAC
ENST00000646208.1:c.223+18_223+19delinsAC	ENSP00000493723.1:n.223+18_223+19delinsAC
ENST00000646410.1:c.358+18_358+19delinsAC	ENSP00000494205.1:n.358+18_358+19delinsAC
ENST00000646562.1:c.*321+18_*321+19delinsAC	ENSP00000496087.1:n.*321+18_*321+19delinsAC
ENST00000647468.2:c.487+18_487+19delinsAC MANE Select	ENSP00000496731.1:n.487+18_487+19delinsAC
ENST00000648111.1:c.*131+18_*131+19delinsAC	ENSP00000497275.1:n.*131+18_*131+19delinsAC
ENST00000367101.5:c.487+18_487+19delinsAC	ENSP00000356068.1:n.487+18_487+19delinsAC
ENST00000367104.7:c.487+18_487+19delinsAC	ENSP00000356071.3:n.487+18_487+19delinsAC
ENST00000606965.5:c.487+18_487+19delinsAC	ENSP00000475808.1:n.487+18_487+19delinsAC
ENST00000607000.1:c.*1_*2delinsAC	ENSP00000475788.1:n.*1_*2delinsAC
ENST00000607071.5:c.*321+18_*321+19delinsAC	ENSP00000475855.1:n.*321+18_*321+19delinsAC
ENST00000607742.5:c.*321+18_*321+19delinsAC	ENSP00000475523.1:n.*321+18_*321+19delinsAC
NM_032861.3:c.487+18_487+19delinsAC	NP_116250.3:n.487+18_487+19delinsAC
NR_073096.1:n.629+18_629+19delinsAC
XM_006715586.1:c.277+18_277+19delinsAC	XP_006715649.1:n.277+18_277+19delinsAC
XM_011536196.1:c.466+18_466+19delinsAC	XP_011534498.1:n.466+18_466+19delinsAC
XM_011536197.1:c.487+18_487+19delinsAC	XP_011534499.1:n.487+18_487+19delinsAC
XM_011536198.1:c.277+18_277+19delinsAC	XP_011534500.1:n.277+18_277+19delinsAC
XR_942606.1:n.488+18_488+19delinsAC
XM_006715586.3:c.277+18_277+19delinsAC	XP_006715649.1:n.277+18_277+19delinsAC
XM_011536196.3:c.466+18_466+19delinsAC	XP_011534498.1:n.466+18_466+19delinsAC
XM_011536198.3:c.277+18_277+19delinsAC	XP_011534500.1:n.277+18_277+19delinsAC
XM_024446573.1:c.487+18_487+19delinsAC	XP_024302341.1:n.487+18_487+19delinsAC
XR_001743697.2:n.568+18_568+19delinsAC
XR_942606.2:n.619+18_619+19delinsAC
NM_032861.4:c.487+18_487+19delinsAC MANE Select	NP_116250.3:n.487+18_487+19delinsAC
NR_073096.2:n.611+18_611+19delinsAC