Canonical Allele Identifier: CA164674077
Gene: IMMP2L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.110700918T>C , CM000669.2:g.110700918T>C GRCh38
NC_000007.13:g.110340974T>C , CM000669.1:g.110340974T>C GRCh37
NC_000007.12:g.110128210T>C NCBI36
NG_030016.1:g.866600A>G
NG_030016.2:g.866600A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405709.7:c.409-37197A>G MANE Select ENSP00000384966.2:n.409-37197A>G
ENST00000331762.7:c.409-37197A>G ENSP00000329553.3:n.409-37197A>G
ENST00000405709.6:c.409-37197A>G ENSP00000384966.2:n.409-37197A>G
ENST00000450877.5:c.355-37197A>G ENSP00000402824.1:n.355-37197A>G
ENST00000452895.5:c.409-37197A>G ENSP00000399353.1:n.409-37197A>G
ENST00000487733.5:n.67-37197A>G
ENST00000489381.1:n.247-35906A>G
NM_001244606.1:c.409-37197A>G NP_001231535.1:n.409-37197A>G
NM_032549.3:c.409-37197A>G NP_115938.1:n.409-37197A>G
XM_005250630.3:c.409-37197A>G XP_005250687.1:n.409-37197A>G
XM_011516605.1:c.493-37197A>G XP_011514907.1:n.493-37197A>G
XM_011516609.1:c.390-37197A>G XP_011514911.1:n.390-37197A>G
XM_011516613.1:c.306-37197A>G XP_011514915.1:n.306-37197A>G
NM_001350959.1:c.409-37197A>G NP_001337888.1:n.409-37197A>G
NM_001350960.1:c.409-37197A>G NP_001337889.1:n.409-37197A>G
NM_001350961.1:c.493-37197A>G NP_001337890.1:n.493-37197A>G
NM_001350963.1:c.306-37197A>G NP_001337892.1:n.306-37197A>G
XM_011516609.2:c.390-37197A>G XP_011514911.1:n.390-37197A>G
XM_024446956.1:c.286-37197A>G XP_024302724.1:n.286-37197A>G
NM_001244606.2:c.409-37197A>G NP_001231535.1:n.409-37197A>G
NM_001350959.2:c.409-37197A>G NP_001337888.1:n.409-37197A>G
NM_001350960.2:c.409-37197A>G NP_001337889.1:n.409-37197A>G
NM_001350961.2:c.493-37197A>G NP_001337890.1:n.493-37197A>G
NM_001350963.2:c.306-37197A>G NP_001337892.1:n.306-37197A>G
NM_032549.4:c.409-37197A>G MANE Select NP_115938.1:n.409-37197A>G
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