Canonical Allele Identifier: CA369643784

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143029835A>T (hg19) ; chr7:g.143332742A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332742A>T , CM000669.2:g.143332742A>T	GRCh38
NC_000007.13:g.143029835A>T , CM000669.1:g.143029835A>T	GRCh37
NC_000007.12:g.142739957A>T	NCBI36
NG_009815.1:g.21617A>T
NG_009815.2:g.21617A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1270A>T	ENSP00000498052.2:p.Ile424Phe
ENST00000343257.7:c.1270A>T MANE Select	ENSP00000339867.2:p.Ile424Phe
ENST00000432192.6:c.1094A>T
ENST00000343257.6:c.1270A>T	ENSP00000339867.2:p.Ile424Phe
NM_000083.2:c.1270A>T	NP_000074.2:p.Ile424Phe
NR_046453.1:n.1341+239A>T
XM_011515781.1:c.1294A>T	XP_011514083.1:p.Ile432Phe
XM_011515782.1:c.16A>T	XP_011514084.1:p.Ile6Phe
XM_011515782.2:c.16A>T	XP_011514084.1:p.Ile6Phe
XM_017011739.1:c.844A>T	XP_016867228.1:p.Ile282Phe
XM_017011740.1:c.820A>T	XP_016867229.1:p.Ile274Phe
NM_000083.3:c.1270A>T MANE Select	NP_000074.3:p.Ile424Phe
NR_046453.2:n.1356+239A>T