Canonical Allele Identifier: CA2643487215

Gene: CTRC

Linked Data

• gnomAD v4: 1-15445554-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445554_15445555insC , CM000663.2:g.15445554_15445555insC	GRCh38
NC_000001.10:g.15772049_15772050insC , CM000663.1:g.15772049_15772050insC	GRCh37
NC_000001.9:g.15644636_15644637insC	NCBI36
NG_009253.1:g.12112_12113insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.640-43_640-42insC MANE Select	ENSP00000365116.4:n.640-43_640-42insC
ENST00000375943.6:c.*94-43_*94-42insC	ENSP00000365110.2:n.*94-43_*94-42insC
ENST00000375949.4:c.640-43_640-42insC	ENSP00000365116.4:n.640-43_640-42insC
ENST00000483406.1:n.404-43_404-42insC
NM_007272.2:c.640-43_640-42insC	NP_009203.2:n.640-43_640-42insC
XM_011540550.1:c.494-43_494-42insC	XP_011538852.1:n.494-43_494-42insC
NM_007272.3:c.640-43_640-42insC MANE Select	NP_009203.2:n.640-43_640-42insC