Canonical Allele Identifier: CA2617686525

Gene: CDKN1B

Linked Data

• gnomAD v4: 12-12718389-G-GTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718389_12718390insTCT , CM000674.2:g.12718389_12718390insTCT	GRCh38
NC_000012.11:g.12871323_12871324insTCT , CM000674.1:g.12871323_12871324insTCT	GRCh37
NC_000012.10:g.12762590_12762591insTCT	NCBI36
NG_016341.1:g.6022_6023insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.475+75_475+76insTCT	ENSP00000507272.1:n.475+75_475+76insTCT
ENST00000682620.1:n.1631-436_1631-435insTCT
ENST00000684771.1:n.585-436_585-435insTCT
ENST00000228872.9:c.475+75_475+76insTCT MANE Select	ENSP00000228872.4:n.475+75_475+76insTCT
ENST00000228872.8:c.475+75_475+76insTCT	ENSP00000228872.4:n.475+75_475+76insTCT
ENST00000396340.1:c.475+75_475+76insTCT	ENSP00000379629.1:n.475+75_475+76insTCT
ENST00000442489.1:c.193+336_193+337insTCT	ENSP00000407597.1:n.193+336_193+337insTCT
ENST00000477087.1:n.155-436_155-435insTCT
NM_004064.4:c.475+75_475+76insTCT	NP_004055.1:n.475+75_475+76insTCT
NM_004064.5:c.475+75_475+76insTCT MANE Select	NP_004055.1:n.475+75_475+76insTCT