Canonical Allele Identifier: CA369645434

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036407T>A (hg19) ; chr7:g.143339314T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339314T>A , CM000669.2:g.143339314T>A	GRCh38
NC_000007.13:g.143036407T>A , CM000669.1:g.143036407T>A	GRCh37
NC_000007.12:g.142746529T>A	NCBI36
NG_009815.1:g.28189T>A
NG_009815.2:g.28189T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1463T>A	ENSP00000498052.2:p.Phe488Tyr
ENST00000343257.7:c.1463T>A MANE Select	ENSP00000339867.2:p.Phe488Tyr
ENST00000432192.6:c.1287T>A
ENST00000343257.6:c.1463T>A	ENSP00000339867.2:p.Phe488Tyr
NM_000083.2:c.1463T>A	NP_000074.2:p.Phe488Tyr
NR_046453.1:n.1403T>A
XM_011515781.1:c.1487T>A	XP_011514083.1:p.Phe496Tyr
XM_011515782.1:c.209T>A	XP_011514084.1:p.Phe70Tyr
XM_011515782.2:c.209T>A	XP_011514084.1:p.Phe70Tyr
XM_017011739.1:c.1037T>A	XP_016867228.1:p.Phe346Tyr
XM_017011740.1:c.1013T>A	XP_016867229.1:p.Phe338Tyr
NM_000083.3:c.1463T>A MANE Select	NP_000074.3:p.Phe488Tyr
NR_046453.2:n.1418T>A