Canonical Allele Identifier: CA673091134

Gene: KIRREL3

Linked Data

• dbSNP Id: rs1211389656
• gnomAD v3: 11-126989205-A-G
• gnomAD v4: 11-126989205-A-G
• MyVariant Identifiers: chr11:g.126859101A>G (hg19) ; chr11:g.126989205A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126989205A>G , CM000673.2:g.126989205A>G	GRCh38
NC_000011.9:g.126859101A>G , CM000673.1:g.126859101A>G	GRCh37
NC_000011.8:g.126364311A>G	NCBI36
NG_012971.1:g.16666T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525144.7:c.55+11250T>C MANE Select	ENSP00000435466.2:n.55+11250T>C
ENST00000525144.6:c.55+11250T>C	ENSP00000435466.2:n.55+11250T>C
ENST00000525704.2:c.55+11250T>C	ENSP00000435094.2:n.55+11250T>C
ENST00000529097.6:c.55+11250T>C	ENSP00000434081.2:n.55+11250T>C
ENST00000533026.6:n.621+11250T>C
ENST00000547738.5:n.711+11250T>C
ENST00000549874.1:n.316+11250T>C
NM_001161707.1:c.55+11250T>C	NP_001155179.1:n.55+11250T>C
NM_001301097.1:c.55+11250T>C	NP_001288026.1:n.55+11250T>C
NM_032531.3:c.55+11250T>C	NP_115920.1:n.55+11250T>C
XM_011543026.1:c.73+11075T>C	XP_011541328.1:n.73+11075T>C
XM_011543027.1:c.55+11250T>C	XP_011541329.1:n.55+11250T>C
XM_011543028.1:c.55+11250T>C	XP_011541330.1:n.55+11250T>C
XM_011543029.1:c.55+11250T>C	XP_011541331.1:n.55+11250T>C
XM_011543030.1:c.73+11075T>C	XP_011541332.1:n.73+11075T>C
XM_011543031.1:c.55+11250T>C	XP_011541333.1:n.55+11250T>C
XM_011543032.1:c.73+11075T>C	XP_011541334.1:n.73+11075T>C
XM_011543033.1:c.55+11250T>C	XP_011541335.1:n.55+11250T>C
XM_011543026.2:c.73+11075T>C	XP_011541328.1:n.73+11075T>C
XM_011543027.2:c.55+11250T>C	XP_011541329.1:n.55+11250T>C
XM_011543028.2:c.55+11250T>C	XP_011541330.1:n.55+11250T>C
XM_011543030.3:c.73+11075T>C	XP_011541332.1:n.73+11075T>C
XM_011543031.2:c.55+11250T>C	XP_011541333.1:n.55+11250T>C
XM_011543032.3:c.73+11075T>C	XP_011541334.1:n.73+11075T>C
XM_017018419.1:c.55+11250T>C	XP_016873908.1:n.55+11250T>C
XM_017018420.1:c.55+11250T>C	XP_016873909.1:n.55+11250T>C
NM_032531.4:c.55+11250T>C MANE Select	NP_115920.1:n.55+11250T>C