Canonical Allele Identifier: CA369643572

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143029587G>T (hg19) ; chr7:g.143332494G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332494G>T , CM000669.2:g.143332494G>T	GRCh38
NC_000007.13:g.143029587G>T , CM000669.1:g.143029587G>T	GRCh37
NC_000007.12:g.142739709G>T	NCBI36
NG_009815.1:g.21369G>T
NG_009815.2:g.21369G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1242G>T	ENSP00000498052.2:p.Met414Ile
ENST00000343257.7:c.1242G>T MANE Select	ENSP00000339867.2:p.Met414Ile
ENST00000432192.6:c.1066G>T
ENST00000343257.6:c.1242G>T	ENSP00000339867.2:p.Met414Ile
NM_000083.2:c.1242G>T	NP_000074.2:p.Met414Ile
NR_046453.1:n.1332G>T
XM_011515781.1:c.1242G>T	XP_011514083.1:p.Met414Ile
XM_011515782.1:c.-3-230G>T	XP_011514084.1:n.-3-230G>T
XM_011515782.2:c.-3-230G>T	XP_011514084.1:n.-3-230G>T
XM_017011739.1:c.792G>T	XP_016867228.1:p.Met264Ile
XM_017011740.1:c.792G>T	XP_016867229.1:p.Met264Ile
NM_000083.3:c.1242G>T MANE Select	NP_000074.3:p.Met414Ile
NR_046453.2:n.1347G>T