Canonical Allele Identifier: CA2536156644

Gene: THSD7B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137469792_137469793insAGCAATA , CM000664.2:g.137469792_137469793insAGCAATA	GRCh38
NC_000002.11:g.138227362_138227363insAGCAATA , CM000664.1:g.138227362_138227363insAGCAATA	GRCh37
NC_000002.10:g.137943832_137943833insAGCAATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409968.6:c.3138+18769_3138+18770insAGCAATA MANE Select	ENSP00000387145.1:n.3138+18769_3138+18770insAGCAATA
ENST00000272643.7:c.3139+18768_3139+18769insAGCAATA	ENSP00000272643.4:n.3139+18768_3139+18769insAGCAATA
ENST00000409968.5:c.3138+18769_3138+18770insAGCAATA	ENSP00000387145.1:n.3138+18769_3138+18770insAGCAATA
ENST00000413152.3:c.3046+18768_3046+18769insAGCAATA	ENSP00000413841.3:n.3046+18768_3046+18769insAGCAATA
NM_001080427.1:c.3045+18769_3045+18770insAGCAATA	NP_001073896.1:n.3045+18769_3045+18770insAGCAATA
NM_001316349.1:c.3138+18769_3138+18770insAGCAATA	NP_001303278.1:n.3138+18769_3138+18770insAGCAATA
XM_017005049.1:c.1341+18769_1341+18770insAGCAATA	XP_016860538.1:n.1341+18769_1341+18770insAGCAATA
NM_001316349.2:c.3138+18769_3138+18770insAGCAATA MANE Select	NP_001303278.1:n.3138+18769_3138+18770insAGCAATA