Canonical Allele Identifier: CA2774746030
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283594_24283595insC , CM000669.2:g.24283594_24283595insC GRCh38
NC_000007.13:g.24323213_24323214insC , CM000669.1:g.24323213_24323214insC GRCh37
NC_000007.12:g.24289738_24289739insC NCBI36
NG_016148.1:g.4407_4408insC

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-27896_42-27895insG XP_016868399.1:n.42-27896_42-27895insG
XM_017012911.1:c.42-27896_42-27895insG XP_016868400.1:n.42-27896_42-27895insG
XR_001745121.1:n.473+35762_473+35763insG
XR_001745122.1:n.345-86566_345-86565insG
XR_001745123.1:n.473+35762_473+35763insG
XR_001745124.1:n.473+35762_473+35763insG
XR_001745125.1:n.473+35762_473+35763insG
XR_001745126.1:n.473+35762_473+35763insG
XR_001745127.1:n.345-27896_345-27895insG
XR_001745129.1:n.473+35762_473+35763insG
XR_001745130.1:n.473+35762_473+35763insG
XR_001745131.1:n.473+35762_473+35763insG
XR_001745132.1:n.473+35762_473+35763insG
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