Canonical Allele Identifier: CA754875186

Gene: LIMS1

Linked Data

• dbSNP Id: rs1456851734
• MyVariant Identifiers: chr2:g.109174643T>C (hg19) ; chr2:g.108558187T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108558187T>C , CM000664.2:g.108558187T>C	GRCh38
NC_000002.11:g.109174643T>C , CM000664.1:g.109174643T>C	GRCh37
NC_000002.10:g.108541075T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000544547.6:c.32+23593T>C MANE Select	ENSP00000437912.1:n.32+23593T>C
ENST00000695516.1:c.59+24379T>C	ENSP00000511979.1:n.59+24379T>C
ENST00000695517.1:c.32+23593T>C	ENSP00000511980.1:n.32+23593T>C
ENST00000428064.5:c.32+23593T>C	ENSP00000390862.1:n.32+23593T>C
ENST00000544547.5:c.32+23593T>C	ENSP00000437912.1:n.32+23593T>C
NM_001193483.2:c.32+23593T>C	NP_001180412.1:n.32+23593T>C
XM_005263949.1:c.32+23593T>C	XP_005264006.1:n.32+23593T>C
XM_017004092.1:c.-84+23593T>C	XP_016859581.1:n.-84+23593T>C
NM_001193483.3:c.32+23593T>C MANE Select	NP_001180412.1:n.32+23593T>C
NM_001371495.1:c.32+23593T>C	NP_001358424.1:n.32+23593T>C
NM_001371496.1:c.59+24379T>C	NP_001358425.1:n.59+24379T>C
NM_001394896.1:c.32+23593T>C	NP_001381825.1:n.32+23593T>C
NM_001394898.1:c.59+24379T>C	NP_001381827.1:n.59+24379T>C