Canonical Allele Identifier: CA1675959075

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114626_158114630delinsCAAAG , CM000668.2:g.158114626_158114630delinsCAAAG	GRCh38
NC_000006.11:g.158535658_158535662delinsCAAAG , CM000668.1:g.158535658_158535662delinsCAAAG	GRCh37
NC_000006.10:g.158455646_158455650delinsCAAAG	NCBI36
NG_032889.1:g.58651_58655delinsCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+159_*1404+163delinsCTTTG	ENSP00000475855.1:n.*1404+159_*1404+163delinsCTTTG
ENST00000642244.1:c.1594+159_1594+163delinsCTTTG	ENSP00000493554.1:n.1594+159_1594+163delinsCTTTG
ENST00000642903.1:c.*79_*83delinsCTTTG	ENSP00000493559.1:n.*79_*83delinsCTTTG
ENST00000644972.1:c.1684+159_1684+163delinsCTTTG	ENSP00000496451.1:n.1684+159_1684+163delinsCTTTG
ENST00000645077.1:c.*1305+159_*1305+163delinsCTTTG	ENSP00000496113.1:n.*1305+159_*1305+163delinsCTTTG
ENST00000645172.1:c.*1386+159_*1386+163delinsCTTTG	ENSP00000495367.1:n.*1386+159_*1386+163delinsCTTTG
ENST00000646190.1:n.3015+159_3015+163delinsCTTTG
ENST00000646208.1:c.1420+159_1420+163delinsCTTTG	ENSP00000493723.1:n.1420+159_1420+163delinsCTTTG
ENST00000646410.1:c.1555+159_1555+163delinsCTTTG	ENSP00000494205.1:n.1555+159_1555+163delinsCTTTG
ENST00000646562.1:c.*1677_*1681delinsCTTTG	ENSP00000496087.1:n.*1677_*1681delinsCTTTG
ENST00000647468.2:c.1684+159_1684+163delinsCTTTG MANE Select	ENSP00000496731.1:n.1684+159_1684+163delinsCTTTG
ENST00000648111.1:c.*1372+159_*1372+163delinsCTTTG	ENSP00000497275.1:n.*1372+159_*1372+163delinsCTTTG
ENST00000367104.7:c.1684+159_1684+163delinsCTTTG	ENSP00000356071.3:n.1684+159_1684+163delinsCTTTG
ENST00000606965.5:c.*404_*408delinsCTTTG	ENSP00000475808.1:n.*404_*408delinsCTTTG
ENST00000607071.5:c.*1618+159_*1618+163delinsCTTTG	ENSP00000475855.1:n.*1618+159_*1618+163delinsCTTTG
ENST00000607742.5:c.*2962+159_*2962+163delinsCTTTG	ENSP00000475523.1:n.*2962+159_*2962+163delinsCTTTG
NM_032861.3:c.1684+159_1684+163delinsCTTTG	NP_116250.3:n.1684+159_1684+163delinsCTTTG
NR_073096.1:n.1776_1780delinsCTTTG
XM_006715586.1:c.1474+159_1474+163delinsCTTTG	XP_006715649.1:n.1474+159_1474+163delinsCTTTG
XM_011536196.1:c.1663+159_1663+163delinsCTTTG	XP_011534498.1:n.1663+159_1663+163delinsCTTTG
XM_011536197.1:c.1570+159_1570+163delinsCTTTG	XP_011534499.1:n.1570+159_1570+163delinsCTTTG
XM_011536198.1:c.1474+159_1474+163delinsCTTTG	XP_011534500.1:n.1474+159_1474+163delinsCTTTG
XM_006715586.3:c.1474+159_1474+163delinsCTTTG	XP_006715649.1:n.1474+159_1474+163delinsCTTTG
XM_011536196.3:c.1663+159_1663+163delinsCTTTG	XP_011534498.1:n.1663+159_1663+163delinsCTTTG
XM_011536198.3:c.1474+159_1474+163delinsCTTTG	XP_011534500.1:n.1474+159_1474+163delinsCTTTG
XM_024446573.1:c.1684+159_1684+163delinsCTTTG	XP_024302341.1:n.1684+159_1684+163delinsCTTTG
XR_001743697.2:n.1715+159_1715+163delinsCTTTG
XR_942606.2:n.1766+159_1766+163delinsCTTTG
NM_032861.4:c.1684+159_1684+163delinsCTTTG MANE Select	NP_116250.3:n.1684+159_1684+163delinsCTTTG
NR_073096.2:n.1758_1762delinsCTTTG