Canonical Allele Identifier: CA393938852

Gene: LINS1

Linked Data

• MyVariant Identifiers: chr15:g.101120968T>C (hg19) ; chr15:g.100580763T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.100580763T>C , CM000677.2:g.100580763T>C	GRCh38
NC_000015.9:g.101120968T>C , CM000677.1:g.101120968T>C	GRCh37
NC_000015.8:g.98938491T>C	NCBI36
NG_034076.1:g.26478A>G
NG_034076.2:g.27270A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314742.13:c.80A>G MANE Select	ENSP00000318423.8:p.Asp27Gly
ENST00000314742.12:c.80A>G	ENSP00000318423.8:p.Asp27Gly
ENST00000559149.5:n.237A>G
ENST00000559577.5:c.80A>G	ENSP00000453642.1:p.Asp27Gly
ENST00000559736.5:c.80A>G	ENSP00000452941.1:p.Asp27Gly
ENST00000560133.5:c.42+38A>G	ENSP00000454929.1:n.42+38A>G
ENST00000560272.1:c.80A>G	ENSP00000453495.1:p.Asp27Gly
ENST00000560934.1:c.80A>G	ENSP00000453692.1:p.Asp27Gly
ENST00000560941.5:c.-137-27A>G	ENSP00000454985.1:n.-137-27A>G
ENST00000561073.1:n.213A>G
ENST00000561308.5:c.80A>G	ENSP00000454200.1:p.Asp27Gly
NM_001040616.2:c.80A>G	NP_001035706.1:p.Asp27Gly
XM_005254941.1:c.80A>G	XP_005254998.1:p.Asp27Gly
XM_005254943.1:c.80A>G	XP_005255000.1:p.Asp27Gly
XR_243210.2:n.183A>G
XR_429464.2:n.183A>G
XR_931862.1:n.183A>G
XR_931863.1:n.183A>G
XR_931864.1:n.183A>G
NM_001352507.1:c.-830A>G	NP_001339436.1:n.-830A>G
NM_001352508.1:c.80A>G	NP_001339437.1:p.Asp27Gly
NR_148017.1:n.303A>G
NR_148018.1:n.303A>G
NR_148019.1:n.307A>G
XM_005254941.2:c.80A>G	XP_005254998.1:p.Asp27Gly
XM_005254943.2:c.80A>G	XP_005255000.1:p.Asp27Gly
XM_017022400.2:c.-830A>G	XP_016877889.1:n.-830A>G
XM_024449979.1:c.80A>G	XP_024305747.1:p.Asp27Gly
XM_024449980.1:c.80A>G	XP_024305748.1:p.Asp27Gly
XR_001751346.2:n.1095A>G
XR_001751347.2:n.1095A>G
XR_001751348.2:n.1095A>G
XR_002957655.1:n.1095A>G
XR_931862.3:n.1095A>G
NM_001040616.3:c.80A>G MANE Select	NP_001035706.2:p.Asp27Gly
NM_001352507.2:c.-830A>G	NP_001339436.1:n.-830A>G
NM_001352508.2:c.80A>G	NP_001339437.1:p.Asp27Gly
NR_148017.2:n.247A>G
NR_148018.2:n.247A>G
NR_148019.2:n.251A>G