Canonical Allele Identifier: CA369645594

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036624G>C (hg19) ; chr7:g.143339531G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339531G>C , CM000669.2:g.143339531G>C	GRCh38
NC_000007.13:g.143036624G>C , CM000669.1:g.143036624G>C	GRCh37
NC_000007.12:g.142746746G>C	NCBI36
NG_009815.1:g.28406G>C
NG_009815.2:g.28406G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1492G>C	ENSP00000498052.2:p.Val498Leu
ENST00000343257.7:c.1492G>C MANE Select	ENSP00000339867.2:p.Val498Leu
ENST00000432192.6:c.1316G>C
ENST00000343257.6:c.1492G>C	ENSP00000339867.2:p.Val498Leu
NM_000083.2:c.1492G>C	NP_000074.2:p.Val498Leu
NR_046453.1:n.1432G>C
XM_011515781.1:c.1516G>C	XP_011514083.1:p.Val506Leu
XM_011515782.1:c.238G>C	XP_011514084.1:p.Val80Leu
XM_011515782.2:c.238G>C	XP_011514084.1:p.Val80Leu
XM_017011739.1:c.1066G>C	XP_016867228.1:p.Val356Leu
XM_017011740.1:c.1042G>C	XP_016867229.1:p.Val348Leu
NM_000083.3:c.1492G>C MANE Select	NP_000074.3:p.Val498Leu
NR_046453.2:n.1447G>C