Canonical Allele Identifier: CA4043728
Gene: LATS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149684479T>C , CM000668.2:g.149684479T>C GRCh38
NC_000006.11:g.150005615T>C , CM000668.1:g.150005615T>C GRCh37
NC_000006.10:g.150047308T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004690.4:c.610A>G MANE Select NP_004681.1:p.Ser204Gly
ENST00000543571.6:c.610A>G MANE Select ENSP00000437550.1:p.Ser204Gly
NM_001270519.1:c.610A>G NP_001257448.1:p.Ser204Gly
NM_001270519.2:c.610A>G NP_001257448.1:p.Ser204Gly
NM_001350339.1:c.295A>G NP_001337268.1:p.Ser99Gly
NM_001350339.2:c.295A>G NP_001337268.1:p.Ser99Gly
NM_001350340.1:c.295A>G NP_001337269.1:p.Ser99Gly
NM_001350340.2:c.295A>G NP_001337269.1:p.Ser99Gly
NM_001350392.1:c.-231A>G NP_001337321.1:n.-231A>G
NM_001350392.2:c.-231A>G NP_001337321.1:n.-231A>G
NM_004690.3:c.610A>G NP_004681.1:p.Ser204Gly
NR_073033.1:n.1064A>G
NR_073033.2:n.1064A>G
ENST00000253339.9:c.610A>G ENSP00000253339.5:p.Ser204Gly
ENST00000392273.7:c.610A>G ENSP00000444678.1:p.Ser204Gly
ENST00000441107.5:c.*297A>G ENSP00000403815.1:n.*297A>G
ENST00000458696.2:c.448A>G ENSP00000441265.1:p.Ser150Gly
ENST00000542720.1:c.*297A>G ENSP00000444535.1:n.*297A>G
ENST00000542747.5:n.447A>G
ENST00000543571.5:c.610A>G ENSP00000437550.1:p.Ser204Gly
XM_006715603.2:c.610A>G XP_006715666.1:p.Ser204Gly
XM_006715603.3:c.610A>G XP_006715666.1:p.Ser204Gly
XM_011536250.1:c.610A>G XP_011534552.1:p.Ser204Gly
XM_011536251.1:c.295A>G XP_011534553.1:p.Ser99Gly
XM_011536252.1:c.610A>G XP_011534554.1:p.Ser204Gly
XM_011536252.2:c.610A>G XP_011534554.1:p.Ser204Gly
XM_017011474.1:c.610A>G XP_016866963.1:p.Ser204Gly
XM_017011477.1:c.610A>G XP_016866966.1:p.Ser204Gly
XM_017011479.1:c.610A>G XP_016866968.1:p.Ser204Gly
XM_017011480.1:c.-231A>G XP_016866969.1:n.-231A>G
XM_017011482.1:c.610A>G XP_016866971.1:p.Ser204Gly
XM_024446583.1:c.610A>G XP_024302351.1:p.Ser204Gly