Canonical Allele Identifier: CA613408
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs373970317
ExAC: 1:15772049 T / TG
gnomAD v2: 1-15772049-T-TG
gnomAD v3: 1-15445554-T-TG
gnomAD v4: 1-15445554-T-TG
MyVariant Identifiers: chr1:g.15772050_15772051insG (hg19) chr1:g.15772049_15772050insG (hg19) chr1:g.15445555_15445556insG (hg38) chr1:g.15445554_15445555insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445563dup , CM000663.2:g.15445563dup GRCh38
NC_000001.10:g.15772058dup , CM000663.1:g.15772058dup GRCh37
NC_000001.9:g.15644645dup NCBI36
NG_009253.1:g.12121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-34dup MANE Select ENSP00000365116.4:n.640-34dup
ENST00000375943.6:c.*94-34dup ENSP00000365110.2:n.*94-34dup
ENST00000375949.4:c.640-34dup ENSP00000365116.4:n.640-34dup
ENST00000483406.1:n.404-34dup
NM_007272.2:c.640-34dup NP_009203.2:n.640-34dup
XM_011540550.1:c.494-34dup XP_011538852.1:n.494-34dup
NM_007272.3:c.640-34dup MANE Select NP_009203.2:n.640-34dup
Search 100 bp 5'
Search 100 bp 3'