Canonical Allele Identifier: CA2612003132

Gene: KCNQ1

Linked Data

• dbSNP Id: rs2133650465
• gnomAD v4: 11-2528159-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2528159G>T , CM000673.2:g.2528159G>T	GRCh38
NC_000011.9:g.2549389G>T , CM000673.1:g.2549389G>T	GRCh37
NC_000011.8:g.2505965G>T	NCBI36
NG_008935.1:g.88169G>T , LRG_287:g.88169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.216+141G>T	ENSP00000434560.2:n.216+141G>T
ENST00000646564.2:c.477+141G>T	ENSP00000495806.2:n.477+141G>T
ENST00000155840.12:c.477+141G>T MANE Select	ENSP00000155840.2:n.477+141G>T
ENST00000335475.6:c.96+141G>T	ENSP00000334497.5:n.96+141G>T
ENST00000646564.1:c.123+141G>T	ENSP00000495806.1:n.123+141G>T
ENST00000155840.9:c.477+141G>T	ENSP00000155840.2:n.477+141G>T
ENST00000335475.5:c.96+141G>T	ENSP00000334497.5:n.96+141G>T
ENST00000496887.6:c.216+141G>T	ENSP00000434560.1:n.216+141G>T
NM_000218.2:c.477+141G>T , LRG_287t1:c.477+141G>T	NP_000209.2:n.477+141G>T
NM_181798.1:c.96+141G>T , LRG_287t2:c.96+141G>T	NP_861463.1:n.96+141G>T
NM_000218.3:c.477+141G>T MANE Select	NP_000209.2:n.477+141G>T