Canonical Allele Identifier: CA349342423

Gene: CHN1

Linked Data

• COSMIC: COSM367265
• MyVariant Identifiers: chr2:g.175664963C>A (hg19) ; chr2:g.174800235C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800235C>A , CM000664.2:g.174800235C>A	GRCh38
NC_000002.11:g.175664963C>A , CM000664.1:g.175664963C>A	GRCh37
NC_000002.10:g.175373209C>A	NCBI36
NG_012642.1:g.210208G>T
NG_012642.2:g.210208G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.886G>T	ENSP00000295497.7:p.Val296Phe
ENST00000295497.12:c.886G>T	ENSP00000295497.7:p.Val296Phe
ENST00000409900.9:c.1261G>T MANE Select	ENSP00000386741.4:p.Val421Phe
ENST00000413882.6:c.715G>T	ENSP00000410496.2:p.Val239Phe
ENST00000443238.6:c.739G>T	ENSP00000409798.2:p.Val247Phe
ENST00000488080.6:n.904G>T
ENST00000650731.1:c.586G>T	ENSP00000499146.1:p.Val196Phe
ENST00000650938.1:c.647G>T
ENST00000651246.1:c.853G>T	ENSP00000498484.1:p.Val285Phe
ENST00000651501.1:c.*708G>T	ENSP00000498894.1:n.*708G>T
ENST00000651717.1:c.*537G>T	ENSP00000499124.1:n.*537G>T
ENST00000652036.1:c.937G>T	ENSP00000499139.1:p.Val313Phe
ENST00000295497.11:c.886G>T	ENSP00000295497.7:p.Val296Phe
ENST00000409156.7:c.1183G>T	ENSP00000386470.3:p.Val395Phe
ENST00000409597.5:c.709G>T	ENSP00000386469.1:p.Val237Phe
ENST00000409900.7:c.1261G>T	ENSP00000386741.3:p.Val421Phe
ENST00000488080.5:n.1112G>T
ENST00000492964.1:n.404G>T
NM_001025201.3:c.1183G>T	NP_001020372.2:p.Val395Phe
NM_001206602.1:c.886G>T	NP_001193531.1:p.Val296Phe
NM_001822.5:c.1261G>T	NP_001813.1:p.Val421Phe
NR_038133.1:n.1127G>T
NM_001025201.4:c.1183G>T	NP_001020372.2:p.Val395Phe
NM_001206602.2:c.886G>T	NP_001193531.1:p.Val296Phe
NM_001371513.1:c.1261G>T	NP_001358442.1:p.Val421Phe
NM_001371514.1:c.1312G>T	NP_001358443.1:p.Val438Phe
NM_001822.7:c.1261G>T MANE Select	NP_001813.1:p.Val421Phe
NR_038133.2:n.1129G>T