Canonical Allele Identifier: CA1675959268

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114753_158114754delinsTA , CM000668.2:g.158114753_158114754delinsTA	GRCh38
NC_000006.11:g.158535785_158535786delinsTA , CM000668.1:g.158535785_158535786delinsTA	GRCh37
NC_000006.10:g.158455773_158455774delinsTA	NCBI36
NG_032889.1:g.58527_58528delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+35_*1404+36delinsTA	ENSP00000475855.1:n.*1404+35_*1404+36delinsTA
ENST00000642244.1:c.1594+35_1594+36delinsTA	ENSP00000493554.1:n.1594+35_1594+36delinsTA
ENST00000642903.1:c.1719_1720delinsTA	ENSP00000493559.1:p.Tyr573=
ENST00000644972.1:c.1684+35_1684+36delinsTA	ENSP00000496451.1:n.1684+35_1684+36delinsTA
ENST00000645077.1:c.*1305+35_*1305+36delinsTA	ENSP00000496113.1:n.*1305+35_*1305+36delinsTA
ENST00000645172.1:c.*1386+35_*1386+36delinsTA	ENSP00000495367.1:n.*1386+35_*1386+36delinsTA
ENST00000646190.1:n.3015+35_3015+36delinsTA
ENST00000646208.1:c.1420+35_1420+36delinsTA	ENSP00000493723.1:n.1420+35_1420+36delinsTA
ENST00000646410.1:c.1555+35_1555+36delinsTA	ENSP00000494205.1:n.1555+35_1555+36delinsTA
ENST00000646562.1:c.*1553_*1554delinsTA	ENSP00000496087.1:n.*1553_*1554delinsTA
ENST00000647468.2:c.1684+35_1684+36delinsTA MANE Select	ENSP00000496731.1:n.1684+35_1684+36delinsTA
ENST00000648111.1:c.*1372+35_*1372+36delinsTA	ENSP00000497275.1:n.*1372+35_*1372+36delinsTA
ENST00000367101.5:c.*167_*168delinsTA	ENSP00000356068.1:n.*167_*168delinsTA
ENST00000367104.7:c.1684+35_1684+36delinsTA	ENSP00000356071.3:n.1684+35_1684+36delinsTA
ENST00000435180.5:c.444_445delinsTA	ENSP00000391168.1:p.Tyr148=
ENST00000606965.5:c.*280_*281delinsTA	ENSP00000475808.1:n.*280_*281delinsTA
ENST00000607071.5:c.*1618+35_*1618+36delinsTA	ENSP00000475855.1:n.*1618+35_*1618+36delinsTA
ENST00000607742.5:c.*2962+35_*2962+36delinsTA	ENSP00000475523.1:n.*2962+35_*2962+36delinsTA
NM_032861.3:c.1684+35_1684+36delinsTA	NP_116250.3:n.1684+35_1684+36delinsTA
NR_073096.1:n.1652_1653delinsTA
XM_006715586.1:c.1474+35_1474+36delinsTA	XP_006715649.1:n.1474+35_1474+36delinsTA
XM_011536196.1:c.1663+35_1663+36delinsTA	XP_011534498.1:n.1663+35_1663+36delinsTA
XM_011536197.1:c.1570+35_1570+36delinsTA	XP_011534499.1:n.1570+35_1570+36delinsTA
XM_011536198.1:c.1474+35_1474+36delinsTA	XP_011534500.1:n.1474+35_1474+36delinsTA
XM_006715586.3:c.1474+35_1474+36delinsTA	XP_006715649.1:n.1474+35_1474+36delinsTA
XM_011536196.3:c.1663+35_1663+36delinsTA	XP_011534498.1:n.1663+35_1663+36delinsTA
XM_011536198.3:c.1474+35_1474+36delinsTA	XP_011534500.1:n.1474+35_1474+36delinsTA
XM_024446573.1:c.1684+35_1684+36delinsTA	XP_024302341.1:n.1684+35_1684+36delinsTA
XR_001743697.2:n.1715+35_1715+36delinsTA
XR_942606.2:n.1766+35_1766+36delinsTA
NM_032861.4:c.1684+35_1684+36delinsTA MANE Select	NP_116250.3:n.1684+35_1684+36delinsTA
NR_073096.2:n.1634_1635delinsTA