Canonical Allele Identifier: CA675202029

Gene: KCNQ1 KCNQ1-AS1

Linked Data

• dbSNP Id: rs1268904069
• gnomAD v3: 11-2848170-T-C
• gnomAD v4: 11-2848170-T-C
• MyVariant Identifiers: chr11:g.2869400T>C (hg19) ; chr11:g.2848170T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2848170T>C , CM000673.2:g.2848170T>C	GRCh38
NC_000011.9:g.2869400T>C , CM000673.1:g.2869400T>C	GRCh37
NC_000011.8:g.2825976T>C	NCBI36
NG_008935.1:g.408180T>C , LRG_287:g.408180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.*167T>C (KCNQ1)	ENSP00000434560.2:n.*167T>C
ENST00000155840.12:c.*167T>C (KCNQ1) MANE Select	ENSP00000155840.2:n.*167T>C
ENST00000335475.6:c.*167T>C (KCNQ1)	ENSP00000334497.5:n.*167T>C
ENST00000526095.2:c.*167T>C (KCNQ1)	ENSP00000494939.1:n.*167T>C
ENST00000155840.9:c.*167T>C (KCNQ1)	ENSP00000155840.2:n.*167T>C
ENST00000335475.5:c.*167T>C (KCNQ1)	ENSP00000334497.5:n.*167T>C
ENST00000526095.1:n.705T>C (KCNQ1)
NM_000218.2:c.*167T>C , LRG_287t1:c.*167T>C (KCNQ1)	NP_000209.2:n.*167T>C
NM_181798.1:c.*167T>C , LRG_287t2:c.*167T>C (KCNQ1)	NP_861463.1:n.*167T>C
NR_130721.1:n.778-7728A>G (KCNQ1-AS1)
NM_000218.3:c.*167T>C (KCNQ1) MANE Select	NP_000209.2:n.*167T>C