Canonical Allele Identifier: CA379140463
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2847906G>C , CM000673.2:g.2847906G>C GRCh38
NC_000011.9:g.2869136G>C , CM000673.1:g.2869136G>C GRCh37
NC_000011.8:g.2825712G>C NCBI36
NG_008935.1:g.407916G>C , LRG_287:g.407916G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1577G>C (KCNQ1) ENSP00000434560.2:p.Gly526Ala
ENST00000155840.12:c.1934G>C (KCNQ1) MANE Select ENSP00000155840.2:p.Gly645Ala
ENST00000335475.6:c.1553G>C (KCNQ1) ENSP00000334497.5:p.Gly518Ala
ENST00000526095.2:c.338G>C (KCNQ1) ENSP00000494939.1:p.Gly113Ala
ENST00000155840.9:c.1934G>C (KCNQ1) ENSP00000155840.2:p.Gly645Ala
ENST00000335475.5:c.1553G>C (KCNQ1) ENSP00000334497.5:p.Gly518Ala
ENST00000526095.1:n.441G>C (KCNQ1)
NM_000218.2:c.1934G>C , LRG_287t1:c.1934G>C (KCNQ1) NP_000209.2:p.Gly645Ala
NM_181798.1:c.1553G>C , LRG_287t2:c.1553G>C (KCNQ1) NP_861463.1:p.Gly518Ala
NR_130721.1:n.778-7464C>G (KCNQ1-AS1)
NM_000218.3:c.1934G>C (KCNQ1) MANE Select NP_000209.2:p.Gly645Ala