Canonical Allele Identifier: CA521020199

Gene: RERE

Linked Data

• ClinVar Variation Id: 2071491
• ClinVar RCV Id: RCV002949321
• dbSNP Id: rs1423582291
• gnomAD v2: 1-8418238-CCACGCTGGGG-C
• gnomAD v3: 1-8358178-CCACGCTGGGG-C
• gnomAD v4: 1-8358178-CCACGCTGGGG-C
• MyVariant Identifiers: chr1:g.8418239_8418248del (hg19) ; chr1:g.8358179_8358188del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358184_8358193del , CM000663.2:g.8358184_8358193del	GRCh38
NC_000001.10:g.8418244_8418253del , CM000663.1:g.8418244_8418253del	GRCh37
NC_000001.9:g.8340831_8340840del	NCBI36
NG_047035.1:g.464504_464513del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2677+8_2677+17del	ENSP00000515651.1:n.2677+8_2677+17del
ENST00000400908.7:c.4339+8_4339+17del MANE Select	ENSP00000383700.2:n.4339+8_4339+17del
ENST00000337907.7:c.4339+8_4339+17del	ENSP00000338629.3:n.4339+8_4339+17del
ENST00000377464.5:c.3535+8_3535+17del	ENSP00000366684.1:n.3535+8_3535+17del
ENST00000400907.6:c.1541-2589_1541-2580del	ENSP00000383699.2:n.1541-2589_1541-2580del
ENST00000400908.6:c.4339+8_4339+17del	ENSP00000383700.2:n.4339+8_4339+17del
ENST00000476556.5:c.2677+8_2677+17del	ENSP00000422246.1:n.2677+8_2677+17del
ENST00000505225.1:c.308-1942_308-1933del	ENSP00000423451.1:n.308-1942_308-1933del
NM_001042681.1:c.4339+8_4339+17del	NP_001036146.1:n.4339+8_4339+17del
NM_001042682.1:c.2677+8_2677+17del	NP_001036147.1:n.2677+8_2677+17del
NM_012102.3:c.4339+8_4339+17del	NP_036234.3:n.4339+8_4339+17del
XM_005263464.1:c.4339+8_4339+17del	XP_005263521.1:n.4339+8_4339+17del
XM_005263466.1:c.3535+8_3535+17del	XP_005263523.1:n.3535+8_3535+17del
XM_006710653.1:c.4339+8_4339+17del	XP_006710716.1:n.4339+8_4339+17del
XM_011541510.1:c.4213+8_4213+17del	XP_011539812.1:n.4213+8_4213+17del
XM_005263464.2:c.4339+8_4339+17del	XP_005263521.1:n.4339+8_4339+17del
XM_011541510.2:c.4213+8_4213+17del	XP_011539812.1:n.4213+8_4213+17del
XM_017001358.1:c.4339+8_4339+17del	XP_016856847.1:n.4339+8_4339+17del
XM_017001359.1:c.4339+8_4339+17del	XP_016856848.1:n.4339+8_4339+17del
NM_001042681.2:c.4339+8_4339+17del MANE Select	NP_001036146.1:n.4339+8_4339+17del
NM_001042682.2:c.2677+8_2677+17del	NP_001036147.1:n.2677+8_2677+17del
NM_012102.4:c.4339+8_4339+17del	NP_036234.3:n.4339+8_4339+17del