Canonical Allele Identifier: CA349342400

Gene: CHN1

Linked Data

• MyVariant Identifiers: chr2:g.175664960A>G (hg19) ; chr2:g.174800232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800232A>G , CM000664.2:g.174800232A>G	GRCh38
NC_000002.11:g.175664960A>G , CM000664.1:g.175664960A>G	GRCh37
NC_000002.10:g.175373206A>G	NCBI36
NG_012642.1:g.210211T>C
NG_012642.2:g.210211T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.889T>C	ENSP00000295497.7:p.Phe297Leu
ENST00000295497.12:c.889T>C	ENSP00000295497.7:p.Phe297Leu
ENST00000409900.9:c.1264T>C MANE Select	ENSP00000386741.4:p.Phe422Leu
ENST00000413882.6:c.718T>C	ENSP00000410496.2:p.Phe240Leu
ENST00000443238.6:c.742T>C	ENSP00000409798.2:p.Phe248Leu
ENST00000488080.6:n.907T>C
ENST00000650731.1:c.589T>C	ENSP00000499146.1:p.Phe197Leu
ENST00000650938.1:c.650T>C
ENST00000651246.1:c.856T>C	ENSP00000498484.1:p.Phe286Leu
ENST00000651501.1:c.*711T>C	ENSP00000498894.1:n.*711T>C
ENST00000651717.1:c.*540T>C	ENSP00000499124.1:n.*540T>C
ENST00000652036.1:c.940T>C	ENSP00000499139.1:p.Phe314Leu
ENST00000295497.11:c.889T>C	ENSP00000295497.7:p.Phe297Leu
ENST00000409156.7:c.1186T>C	ENSP00000386470.3:p.Phe396Leu
ENST00000409597.5:c.712T>C	ENSP00000386469.1:p.Phe238Leu
ENST00000409900.7:c.1264T>C	ENSP00000386741.3:p.Phe422Leu
ENST00000488080.5:n.1115T>C
ENST00000492964.1:n.407T>C
NM_001025201.3:c.1186T>C	NP_001020372.2:p.Phe396Leu
NM_001206602.1:c.889T>C	NP_001193531.1:p.Phe297Leu
NM_001822.5:c.1264T>C	NP_001813.1:p.Phe422Leu
NR_038133.1:n.1130T>C
NM_001025201.4:c.1186T>C	NP_001020372.2:p.Phe396Leu
NM_001206602.2:c.889T>C	NP_001193531.1:p.Phe297Leu
NM_001371513.1:c.1264T>C	NP_001358442.1:p.Phe422Leu
NM_001371514.1:c.1315T>C	NP_001358443.1:p.Phe439Leu
NM_001822.7:c.1264T>C MANE Select	NP_001813.1:p.Phe422Leu
NR_038133.2:n.1132T>C