Canonical Allele Identifier: CA2553062519

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866429_72866430insTTTT , CM000670.2:g.72866429_72866430insTTTT	GRCh38
NC_000008.10:g.73778664_73778665insTTTT , CM000670.1:g.73778664_73778665insTTTT	GRCh37
NC_000008.9:g.73941218_73941219insTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000523207.2:c.580-69506_580-69505insTTTT MANE Select	ENSP00000430846.1:n.580-69506_580-69505in...
ENST00000523207.1:c.580-69506_580-69505insTTTT	ENSP00000430846.1:n.580-69506_580-69505in...
NM_004770.2:c.580-69506_580-69505insTTTT	NP_004761.2:n.580-69506_580-69505insTTTT
XM_017013981.1:c.-157+2725_-157+2726insTTTT	XP_016869470.1:n.-157+2725_-157+2726insTT...
XR_001745620.1:n.1141-69506_1141-69505insTTTT
XR_001745621.1:n.1141-69506_1141-69505insTTTT
NM_004770.3:c.580-69506_580-69505insTTTT MANE Select	NP_004761.2:n.580-69506_580-69505insTTTT