Canonical Allele Identifier: CA564379680

Gene: TENM2

Linked Data

• gnomAD v2: 5-166471090-GACTGTTCT-G
• gnomAD v3: 5-167044085-GACTGTTCT-G
• gnomAD v4: 5-167044085-GACTGTTCT-G
• MyVariant Identifiers: chr5:g.166471091_166471098del (hg19) ; chr5:g.167044086_167044093del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167044087_167044094del , CM000667.2:g.167044087_167044094del	GRCh38
NC_000005.9:g.166471092_166471099del , CM000667.1:g.166471092_166471099del	GRCh37
NC_000005.8:g.166403670_166403677del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.-189-29155_-189-29148del MANE Select	ENSP00000429430.1:n.-189-29155_-189-29148...
ENST00000695884.1:n.464-29155_464-29148del
XM_005265950.1:c.-189-29155_-189-29148del	XP_005266007.1:n.-189-29155_-189-29148del...
XM_006714897.1:c.-189-29155_-189-29148del	XP_006714960.1:n.-189-29155_-189-29148del...
XM_011534604.1:c.-189-29155_-189-29148del	XP_011532906.1:n.-189-29155_-189-29148del...
XM_005265950.2:c.-189-29155_-189-29148del	XP_005266007.1:n.-189-29155_-189-29148del...
XM_006714897.2:c.-189-29155_-189-29148del	XP_006714960.1:n.-189-29155_-189-29148del...
XM_011534604.2:c.-189-29155_-189-29148del	XP_011532906.1:n.-189-29155_-189-29148del...
XM_017009660.1:c.-189-29155_-189-29148del	XP_016865149.1:n.-189-29155_-189-29148del...
XM_017009661.1:c.-189-29155_-189-29148del	XP_016865150.1:n.-189-29155_-189-29148del...
XM_017009662.1:c.-189-29155_-189-29148del	XP_016865151.1:n.-189-29155_-189-29148del...
NM_001395460.1:c.-189-29155_-189-29148del MANE Select	NP_001382389.1:n.-189-29155_-189-29148del...