Canonical Allele Identifier: CA14355849
Gene: IQCK HGNC NCBI

Linked Data

dbSNP Id: rs1858973

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.19732327T>C , CM000678.2:g.19732327T>C GRCh38
NC_000016.9:g.19743649T>C , CM000678.1:g.19743649T>C GRCh37
NC_000016.8:g.19651150T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000695302.1:c.247-1371T>C MANE Select ENSP00000511791.1:n.247-1371T>C
ENST00000308214.13:c.247-1371T>C ENSP00000309261.9:n.247-1371T>C
ENST00000320394.10:c.247-1371T>C ENSP00000324901.6:n.247-1371T>C
ENST00000561839.5:c.239-1371T>C
ENST00000561935.5:c.227-1371T>C
ENST00000564186.5:c.247-1371T>C ENSP00000458669.1:n.247-1371T>C
ENST00000564515.5:n.256-1371T>C
ENST00000564955.5:c.182-1371T>C ENSP00000456448.1:n.182-1371T>C
ENST00000566312.1:n.138-1371T>C
ENST00000568126.5:c.182-1371T>C ENSP00000457519.1:n.182-1371T>C
ENST00000568300.6:n.271-1371T>C
NM_001305121.1:c.-18-1371T>C NP_001292050.1:n.-18-1371T>C
NM_001305122.1:c.247-1371T>C NP_001292051.1:n.247-1371T>C
NM_153208.1:c.247-1371T>C NP_694940.1:n.247-1371T>C
NM_153208.2:c.247-1371T>C NP_694940.1:n.247-1371T>C
NR_130967.1:n.946-1371T>C
NR_130968.1:n.946-1371T>C
XM_011545734.1:c.247-1371T>C XP_011544036.1:n.247-1371T>C
XM_011545736.1:c.-18-1371T>C XP_011544038.1:n.-18-1371T>C
XR_950742.1:n.281-1371T>C
XM_011545736.3:c.-18-1371T>C XP_011544038.1:n.-18-1371T>C
NM_001305121.2:c.-18-1371T>C NP_001292050.1:n.-18-1371T>C
NM_001305122.2:c.247-1371T>C NP_001292051.1:n.247-1371T>C
NR_130967.2:n.946-1371T>C
NR_130968.2:n.946-1371T>C
NM_001305121.3:c.-18-1371T>C NP_001292050.1:n.-18-1371T>C
NM_001305122.3:c.247-1371T>C NP_001292051.1:n.247-1371T>C
NM_001394804.1:c.247-1371T>C NP_001381733.1:n.247-1371T>C
NM_001394805.1:c.-18-1371T>C NP_001381734.1:n.-18-1371T>C
NM_001394806.1:c.247-1371T>C NP_001381735.1:n.247-1371T>C
NM_153208.3:c.247-1371T>C MANE Select NP_694940.1:n.247-1371T>C
NR_130967.3:n.283-1371T>C
NR_130968.3:n.283-1371T>C