Canonical Allele Identifier: CA1143963609

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445555_15445563delinsGGGGGGGGG , CM000663.2:g.15445555_15445563delinsGGGGGGGGG	GRCh38
NC_000001.10:g.15772050_15772058delinsGGGGGGGGG , CM000663.1:g.15772050_15772058delinsGGGGGGGGG	GRCh37
NC_000001.9:g.15644637_15644645delinsGGGGGGGGG	NCBI36
NG_009253.1:g.12113_12121delinsGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.640-42_640-34delinsGGGGGGGGG MANE Select	ENSP00000365116.4:n.640-42_640-34delinsGGGGGGGGG
ENST00000375943.6:c.*94-42_*94-34delinsGGGGGGGGG	ENSP00000365110.2:n.*94-42_*94-34delinsGGGGGGGGG
ENST00000375949.4:c.640-42_640-34delinsGGGGGGGGG	ENSP00000365116.4:n.640-42_640-34delinsGGGGGGGGG
ENST00000483406.1:n.404-42_404-34delinsGGGGGGGGG
NM_007272.2:c.640-42_640-34delinsGGGGGGGGG	NP_009203.2:n.640-42_640-34delinsGGGGGGGGG
XM_011540550.1:c.494-42_494-34delinsGGGGGGGGG	XP_011538852.1:n.494-42_494-34delinsGGGGGGGGG
NM_007272.3:c.640-42_640-34delinsGGGGGGGGG MANE Select	NP_009203.2:n.640-42_640-34delinsGGGGGGGGG