Canonical Allele Identifier: CA366022814

Gene: LATS1

Linked Data

• MyVariant Identifiers: chr6:g.150001213C>G (hg19) ; chr6:g.149680077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149680077C>G , CM000668.2:g.149680077C>G	GRCh38
NC_000006.11:g.150001213C>G , CM000668.1:g.150001213C>G	GRCh37
NC_000006.10:g.150042906C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543571.6:c.2391G>C MANE Select	ENSP00000437550.1:p.Met797Ile
ENST00000253339.9:c.2391G>C	ENSP00000253339.5:p.Met797Ile
ENST00000441107.5:c.*2078G>C	ENSP00000403815.1:n.*2078G>C
ENST00000542747.5:n.2228G>C
ENST00000543571.5:c.2391G>C	ENSP00000437550.1:p.Met797Ile
NM_004690.3:c.2391G>C	NP_004681.1:p.Met797Ile
NR_073033.1:n.2845G>C
XM_006715603.2:c.2391G>C	XP_006715666.1:p.Met797Ile
XM_011536250.1:c.2391G>C	XP_011534552.1:p.Met797Ile
XM_011536251.1:c.2076G>C	XP_011534553.1:p.Met692Ile
XM_011536252.1:c.2391G>C	XP_011534554.1:p.Met797Ile
NM_001350339.1:c.2076G>C	NP_001337268.1:p.Met692Ile
NM_001350340.1:c.2076G>C	NP_001337269.1:p.Met692Ile
NM_001350392.1:c.1551G>C	NP_001337321.1:p.Met517Ile
XM_006715603.3:c.2391G>C	XP_006715666.1:p.Met797Ile
XM_011536252.2:c.2391G>C	XP_011534554.1:p.Met797Ile
XM_017011474.1:c.2391G>C	XP_016866963.1:p.Met797Ile
XM_017011477.1:c.2391G>C	XP_016866966.1:p.Met797Ile
XM_017011479.1:c.2391G>C	XP_016866968.1:p.Met797Ile
XM_017011480.1:c.1551G>C	XP_016866969.1:p.Met517Ile
XM_024446583.1:c.2391G>C	XP_024302351.1:p.Met797Ile
NM_004690.4:c.2391G>C MANE Select	NP_004681.1:p.Met797Ile
NM_001350339.2:c.2076G>C	NP_001337268.1:p.Met692Ile
NM_001350340.2:c.2076G>C	NP_001337269.1:p.Met692Ile
NM_001350392.2:c.1551G>C	NP_001337321.1:p.Met517Ile
NR_073033.2:n.2845G>C