Canonical Allele Identifier: CA369646722

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039199T>C (hg19) ; chr7:g.143342106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342106T>C , CM000669.2:g.143342106T>C	GRCh38
NC_000007.13:g.143039199T>C , CM000669.1:g.143039199T>C	GRCh37
NC_000007.12:g.142749321T>C	NCBI36
NG_009815.1:g.30981T>C
NG_009815.2:g.30981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1760T>C	ENSP00000498052.2:p.Leu587Pro
ENST00000343257.7:c.1760T>C MANE Select	ENSP00000339867.2:p.Leu587Pro
ENST00000432192.6:c.1584T>C
ENST00000343257.6:c.1760T>C	ENSP00000339867.2:p.Leu587Pro
NM_000083.2:c.1760T>C	NP_000074.2:p.Leu587Pro
NR_046453.1:n.1700T>C
XM_011515781.1:c.1784T>C	XP_011514083.1:p.Leu595Pro
XM_011515782.1:c.506T>C	XP_011514084.1:p.Leu169Pro
XM_011515782.2:c.506T>C	XP_011514084.1:p.Leu169Pro
XM_017011739.1:c.1334T>C	XP_016867228.1:p.Leu445Pro
XM_017011740.1:c.1310T>C	XP_016867229.1:p.Leu437Pro
NM_000083.3:c.1760T>C MANE Select	NP_000074.3:p.Leu587Pro
NR_046453.2:n.1715T>C