Canonical Allele Identifier: CA82022123
Gene: LSAMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.116021872A>G , CM000665.2:g.116021872A>G GRCh38
NC_000003.11:g.115740719A>G , CM000665.1:g.115740719A>G GRCh37
NC_000003.10:g.117223409A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000490035.7:c.389-2232T>C MANE Select ENSP00000419000.1:n.389-2232T>C
ENST00000333617.8:c.341-2232T>C ENSP00000328455.4:n.341-2232T>C
ENST00000474851.1:c.491-2232T>C ENSP00000418506.1:n.491-2232T>C
ENST00000490035.6:c.389-2232T>C ENSP00000419000.1:n.389-2232T>C
ENST00000498645.1:n.98-2232T>C
ENST00000539563.5:c.239-2232T>C ENSP00000443429.2:n.239-2232T>C
NM_002338.3:c.389-2232T>C NP_002329.2:n.389-2232T>C
XM_005247454.2:c.389-2232T>C XP_005247511.1:n.389-2232T>C
XM_011512838.1:c.389-2232T>C XP_011511140.1:n.389-2232T>C
XM_011512839.1:c.389-2232T>C XP_011511141.1:n.389-2232T>C
XM_011512840.1:c.389-2232T>C XP_011511142.1:n.389-2232T>C
XR_924139.1:n.900-2232T>C
NM_001318915.1:c.389-2232T>C NP_001305844.1:n.389-2232T>C
NM_002338.4:c.389-2232T>C NP_002329.2:n.389-2232T>C
XM_011512840.3:c.389-2232T>C XP_011511142.1:n.389-2232T>C
XM_017006383.2:c.389-2232T>C XP_016861872.1:n.389-2232T>C
XM_024453520.1:c.98-2232T>C XP_024309288.1:n.98-2232T>C
XM_024453521.1:c.98-2232T>C XP_024309289.1:n.98-2232T>C
NM_002338.5:c.389-2232T>C MANE Select NP_002329.2:n.389-2232T>C
NM_001318915.2:c.389-2232T>C NP_001305844.1:n.389-2232T>C
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