Canonical Allele Identifier: CA1227458726

Gene: SIPA1L2

Linked Data

• dbSNP Id: rs1662738537

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.232620372_232620383del , CM000663.2:g.232620372_232620383del	GRCh38
NC_000001.10:g.232756118_232756129del , CM000663.1:g.232756118_232756129del	GRCh37
NC_000001.9:g.230822741_230822752del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674635.1:c.-319+9486_-319+9497del MANE Select	ENSP00000502693.1:n.-319+9486_-319+9497del
ENST00000674749.1:c.-575+9486_-575+9497del	ENSP00000502328.1:n.-575+9486_-575+9497del
ENST00000674801.1:c.-319+10047_-319+10058del	ENSP00000502186.1:n.-319+10047_-319+10058del
ENST00000675407.1:c.-396+9486_-396+9497del	ENSP00000502580.1:n.-396+9486_-396+9497del
ENST00000675685.1:c.-319+10047_-319+10058del	ENSP00000501553.1:n.-319+10047_-319+10058del
ENST00000676213.1:c.-270+10047_-270+10058del	ENSP00000501897.1:n.-270+10047_-270+10058del
XM_005273211.1:c.-319+9486_-319+9497del	XP_005273268.1:n.-319+9486_-319+9497del
XM_005273212.3:c.-347+9486_-347+9497del	XP_005273269.1:n.-347+9486_-347+9497del
XM_005273213.3:c.-270+9486_-270+9497del	XP_005273270.1:n.-270+9486_-270+9497del
XM_006711798.2:c.-413+9486_-413+9497del	XP_006711861.1:n.-413+9486_-413+9497del
XM_011544242.1:c.-490+9486_-490+9497del	XP_011542544.1:n.-490+9486_-490+9497del
XM_011544243.1:c.-396+9486_-396+9497del	XP_011542545.1:n.-396+9486_-396+9497del
XM_011544244.1:c.-270+10047_-270+10058del	XP_011542546.1:n.-270+10047_-270+10058del
XM_011544245.1:c.-490+9486_-490+9497del	XP_011542547.1:n.-490+9486_-490+9497del
XM_005273211.2:c.-319+9486_-319+9497del	XP_005273268.1:n.-319+9486_-319+9497del
XM_005273212.4:c.-347+9486_-347+9497del	XP_005273269.1:n.-347+9486_-347+9497del
XM_005273213.4:c.-270+9486_-270+9497del	XP_005273270.1:n.-270+9486_-270+9497del
XM_011544243.2:c.-396+9486_-396+9497del	XP_011542545.1:n.-396+9486_-396+9497del
XM_017001896.1:c.-319+10047_-319+10058del	XP_016857385.1:n.-319+10047_-319+10058del
XM_017001897.2:c.-319+9486_-319+9497del	XP_016857386.1:n.-319+9486_-319+9497del
XM_017001898.2:c.-319+10047_-319+10058del	XP_016857387.1:n.-319+10047_-319+10058del
NM_001377488.1:c.-319+10047_-319+10058del	NP_001364417.1:n.-319+10047_-319+10058del
NM_020808.5:c.-319+9486_-319+9497del MANE Select	NP_065859.3:n.-319+9486_-319+9497del