Canonical Allele Identifier: CA10709532

Gene: SPMIP3

Linked Data

• dbSNP Id: rs10803209
• gnomAD v2: 1-244533134-A-C
• gnomAD v3: 1-244369832-A-C
• gnomAD v4: 1-244369832-A-C
• MyVariant Identifiers: chr1:g.244533134A>C (hg19) ; chr1:g.244369832A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244369832A>C , CM000663.2:g.244369832A>C	GRCh38
NC_000001.10:g.244533134A>C , CM000663.1:g.244533134A>C	GRCh37
NC_000001.9:g.242599757A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308105.5:c.56+5076A>C MANE Select	ENSP00000311218.4:n.56+5076A>C
ENST00000308105.4:c.56+5076A>C	ENSP00000311218.4:n.56+5076A>C
ENST00000366537.5:c.56+5076A>C	ENSP00000355495.1:n.56+5076A>C
ENST00000486803.1:n.155+5076A>C
NM_001012970.2:c.56+5076A>C	NP_001012988.1:n.56+5076A>C
NM_001276348.1:c.56+5076A>C	NP_001263277.1:n.56+5076A>C
NM_001276349.1:c.56+5076A>C	NP_001263278.1:n.56+5076A>C
XM_011544123.1:c.98+5076A>C	XP_011542425.1:n.98+5076A>C
XM_011544124.1:c.98+5076A>C	XP_011542426.1:n.98+5076A>C
XM_011544125.1:c.56+5076A>C	XP_011542427.1:n.56+5076A>C
XM_011544126.1:c.56+5076A>C	XP_011542428.1:n.56+5076A>C
XM_011544127.1:c.56+5076A>C	XP_011542429.1:n.56+5076A>C
XM_011544128.1:c.56+5076A>C	XP_011542430.1:n.56+5076A>C
XM_011544129.1:c.98+5076A>C	XP_011542431.1:n.98+5076A>C
XM_011544130.1:c.98+5076A>C	XP_011542432.1:n.98+5076A>C
XR_949346.1:n.576+5520T>G
XR_949347.1:n.573+5520T>G
XM_011544124.2:c.98+5076A>C	XP_011542426.1:n.98+5076A>C
XM_011544125.2:c.56+5076A>C	XP_011542427.1:n.56+5076A>C
XM_011544128.2:c.56+5076A>C	XP_011542430.1:n.56+5076A>C
XM_011544129.3:c.98+5076A>C	XP_011542431.1:n.98+5076A>C
XM_011544130.2:c.98+5076A>C	XP_011542432.1:n.98+5076A>C
XM_017000571.2:c.98+5076A>C	XP_016856060.1:n.98+5076A>C
XM_017000572.1:c.98+5076A>C	XP_016856061.1:n.98+5076A>C
NM_001012970.3:c.56+5076A>C MANE Select	NP_001012988.1:n.56+5076A>C
NM_001276348.2:c.56+5076A>C	NP_001263277.1:n.56+5076A>C
NM_001276349.2:c.56+5076A>C	NP_001263278.1:n.56+5076A>C