Canonical Allele Identifier: CA916715025

Gene: CHN1

Linked Data

• dbSNP Id: rs1558927132

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799339_174799340dup , CM000664.2:g.174799339_174799340dup	GRCh38
NC_000002.11:g.175664067_175664068dup , CM000664.1:g.175664067_175664068dup	GRCh37
NC_000002.10:g.175372313_175372314dup	NCBI36
NG_012642.1:g.211104_211105dup
NG_012642.2:g.211104_211105dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.*777_*778dup	ENSP00000295497.7:n.*777_*778dup
ENST00000295497.12:c.*777_*778dup	ENSP00000295497.7:n.*777_*778dup
ENST00000409900.9:c.*777_*778dup MANE Select	ENSP00000386741.4:n.*777_*778dup
NM_001025201.3:c.*777_*778dup	NP_001020372.2:n.*777_*778dup
NM_001206602.1:c.*777_*778dup	NP_001193531.1:n.*777_*778dup
NM_001822.5:c.*777_*778dup	NP_001813.1:n.*777_*778dup
NR_038133.1:n.2023_2024dup
NM_001025201.4:c.*777_*778dup	NP_001020372.2:n.*777_*778dup
NM_001206602.2:c.*777_*778dup	NP_001193531.1:n.*777_*778dup
NM_001371513.1:c.*777_*778dup	NP_001358442.1:n.*777_*778dup
NM_001371514.1:c.*777_*778dup	NP_001358443.1:n.*777_*778dup
NM_001822.7:c.*777_*778dup MANE Select	NP_001813.1:n.*777_*778dup
NR_038133.2:n.2025_2026dup