Canonical Allele Identifier: CA112508134

Gene: TENM3

Linked Data

• dbSNP Id: rs1022526995
• gnomAD v3: 4-181688868-TTC-T
• gnomAD v4: 4-181688868-TTC-T
• MyVariant Identifiers: chr4:g.182610022_182610023del (hg19) ; chr4:g.181688869_181688870del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.181688870_181688871del , CM000666.2:g.181688870_181688871del	GRCh38
NC_000004.11:g.182610023_182610024del , CM000666.1:g.182610023_182610024del	GRCh37
NC_000004.10:g.182847017_182847018del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939532.1:n.155-50617_155-50616del
XM_017008385.1:c.-399-50617_-399-50616del	XP_016863874.1:n.-399-50617_-399-50616del
XM_017008389.1:c.-399-50617_-399-50616del	XP_016863878.1:n.-399-50617_-399-50616del
XM_017008390.1:c.-399-50617_-399-50616del	XP_016863879.1:n.-399-50617_-399-50616del
XM_017008391.1:c.-399-50617_-399-50616del	XP_016863880.1:n.-399-50617_-399-50616del
XM_017008392.1:c.-399-50617_-399-50616del	XP_016863881.1:n.-399-50617_-399-50616del
XM_017008393.1:c.-399-50617_-399-50616del	XP_016863882.1:n.-399-50617_-399-50616del
XM_017008394.1:c.-399-50617_-399-50616del	XP_016863883.1:n.-399-50617_-399-50616del