Canonical Allele Identifier: CA338567767
Gene: CTRC HGNC NCBI

Linked Data

gnomAD v4: 1-15445644-G-A
MyVariant Identifiers: chr1:g.15772139G>A (hg19) chr1:g.15445644G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445644G>A , CM000663.2:g.15445644G>A GRCh38
NC_000001.10:g.15772139G>A , CM000663.1:g.15772139G>A GRCh37
NC_000001.9:g.15644726G>A NCBI36
NG_009253.1:g.12202G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.687G>A MANE Select ENSP00000365116.4:p.Trp229Ter
ENST00000375943.6:c.*141G>A ENSP00000365110.2:n.*141G>A
ENST00000375949.4:c.687G>A ENSP00000365116.4:p.Trp229Ter
ENST00000483406.1:n.451G>A
NM_007272.2:c.687G>A NP_009203.2:p.Trp229Ter
XM_011540550.1:c.541G>A XP_011538852.1:p.Gly181Arg
NM_007272.3:c.687G>A MANE Select NP_009203.2:p.Trp229Ter
Search 100 bp 5'
Search 100 bp 3'