Canonical Allele Identifier: CA4071347

Gene: SERAC1

Linked Data

• dbSNP Id: rs748639508
• ExAC: 6:158567774 CCAG / C
• gnomAD v2: 6-158567774-CCAG-C
• gnomAD v3: 6-158146742-CCAG-C
• gnomAD v4: 6-158146742-CCAG-C
• MyVariant Identifiers: chr6:g.158567775_158567777del (hg19) ; chr6:g.158146744_158146746del (hg38) ; chr6:g.158146743_158146745del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146744_158146746del , CM000668.2:g.158146744_158146746del	GRCh38
NC_000006.11:g.158567776_158567778del , CM000668.1:g.158567776_158567778del	GRCh37
NC_000006.10:g.158487764_158487766del	NCBI36
NG_032889.1:g.26536_26538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*321+37_*321+39del	ENSP00000475855.1:n.*321+37_*321+39del
ENST00000642244.1:c.397+37_397+39del	ENSP00000493554.1:n.397+37_397+39del
ENST00000642903.1:c.487+37_487+39del	ENSP00000493559.1:n.487+37_487+39del
ENST00000644972.1:c.487+37_487+39del	ENSP00000496451.1:n.487+37_487+39del
ENST00000645077.1:c.*321+37_*321+39del	ENSP00000496113.1:n.*321+37_*321+39del
ENST00000645172.1:c.*189+2120_*189+2122del	ENSP00000495367.1:n.*189+2120_*189+2122del
ENST00000646190.1:n.1718+37_1718+39del
ENST00000646208.1:c.223+37_223+39del	ENSP00000493723.1:n.223+37_223+39del
ENST00000646410.1:c.358+37_358+39del	ENSP00000494205.1:n.358+37_358+39del
ENST00000646562.1:c.*321+37_*321+39del	ENSP00000496087.1:n.*321+37_*321+39del
ENST00000647468.2:c.487+37_487+39del MANE Select	ENSP00000496731.1:n.487+37_487+39del
ENST00000648111.1:c.*131+37_*131+39del	ENSP00000497275.1:n.*131+37_*131+39del
ENST00000367101.5:c.487+37_487+39del	ENSP00000356068.1:n.487+37_487+39del
ENST00000367104.7:c.487+37_487+39del	ENSP00000356071.3:n.487+37_487+39del
ENST00000606965.5:c.487+37_487+39del	ENSP00000475808.1:n.487+37_487+39del
ENST00000607000.1:c.*20_*22del	ENSP00000475788.1:n.*20_*22del
ENST00000607071.5:c.*321+37_*321+39del	ENSP00000475855.1:n.*321+37_*321+39del
ENST00000607742.5:c.*321+37_*321+39del	ENSP00000475523.1:n.*321+37_*321+39del
NM_032861.3:c.487+37_487+39del	NP_116250.3:n.487+37_487+39del
NR_073096.1:n.629+37_629+39del
XM_006715586.1:c.277+37_277+39del	XP_006715649.1:n.277+37_277+39del
XM_011536196.1:c.466+37_466+39del	XP_011534498.1:n.466+37_466+39del
XM_011536197.1:c.487+37_487+39del	XP_011534499.1:n.487+37_487+39del
XM_011536198.1:c.277+37_277+39del	XP_011534500.1:n.277+37_277+39del
XR_942606.1:n.488+37_488+39del
XM_006715586.3:c.277+37_277+39del	XP_006715649.1:n.277+37_277+39del
XM_011536196.3:c.466+37_466+39del	XP_011534498.1:n.466+37_466+39del
XM_011536198.3:c.277+37_277+39del	XP_011534500.1:n.277+37_277+39del
XM_024446573.1:c.487+37_487+39del	XP_024302341.1:n.487+37_487+39del
XR_001743697.2:n.568+37_568+39del
XR_942606.2:n.619+37_619+39del
NM_032861.4:c.487+37_487+39del MANE Select	NP_116250.3:n.487+37_487+39del
NR_073096.2:n.611+37_611+39del