Canonical Allele Identifier: CA837065912

Gene:

Linked Data

• dbSNP Id: rs1391483148
• MyVariant Identifiers: chr7:g.26008090_26008091del (hg19) ; chr7:g.25968470_25968471del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.25968472_25968473del , CM000669.2:g.25968472_25968473del	GRCh38
NC_000007.13:g.26008092_26008093del , CM000669.1:g.26008092_26008093del	GRCh37
NC_000007.12:g.25974617_25974618del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927113.1:n.1492-12972_1492-12971del
XR_927114.1:n.1492-29010_1492-29009del
XR_927115.1:n.1583-12972_1583-12971del
XR_927116.1:n.983-12972_983-12971del
XR_927117.1:n.1336-12972_1336-12971del
XR_927118.1:n.1580-12972_1580-12971del
XR_927119.1:n.1243-12972_1243-12971del
XR_927120.1:n.1228-29010_1228-29009del
XR_927122.1:n.718-29010_718-29009del
XR_927123.1:n.1201-12972_1201-12971del
XR_927113.2:n.1519-12972_1519-12971del
XR_927114.2:n.1519-29010_1519-29009del
XR_927116.2:n.1013-12972_1013-12971del
XR_927117.2:n.1364-12972_1364-12971del
XR_927119.2:n.1850-12972_1850-12971del
XR_927120.2:n.1256-29010_1256-29009del
XR_927122.2:n.750-29010_750-29009del
XR_927123.2:n.1224-12972_1224-12971del