Canonical Allele Identifier: CA645509430

Gene: TRPM6

Linked Data

• ClinVar Variation Id: 438256
• ClinVar RCV Id: RCV000504942 ; RCV001003860
• MyVariant Identifiers: chr9:g.77388717_77398576del (hg19) ; chr9:g.74773801_74783660del (hg38)
• PubMed: PMID:28041643

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74773801_74783660del , CM000671.2:g.74773801_74783660del	GRCh38
NC_000009.11:g.77388717_77398576del , CM000671.1:g.77388717_77398576del	GRCh37
NC_000009.10:g.76578537_76588396del	NCBI36
NG_017036.1:g.109436_119295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.2920-806_3404-1965del
ENST00000360774.5:c.2920-806_3404-1965del
ENST00000361255.7:c.2905-806_3389-1965del
ENST00000449912.6:c.2905-806_3389-1965del
NM_001177310.1:c.2905-806_3389-1965del
NM_001177311.1:c.2905-806_3389-1965del
NM_017662.4:c.2920-806_3404-1965del
XM_011518244.1:c.2920-806_3404-1965del
XM_011518245.1:c.2827-806_3311-1965del
XM_011518246.1:c.2920-806_3404-1965del
XM_011518247.1:c.2791-806_3275-1965del
XM_011518248.1:c.2779-806_3263-1965del
XM_011518249.1:c.2686-806_3170-1965del
XM_011518250.1:c.2644-806_3128-1965del
XM_011518251.1:c.2191-806_2675-1965del
XM_011518252.1:c.2920-806_3404-1965del
XM_011518253.1:c.853-806_1337-1965del
XM_011518254.1:c.2920-806_3404-1965del
XM_011518255.1:c.2920-806_3404-1965del
XR_929716.1:n.3158-806_3642-1965del
XR_929717.1:n.3158-806_3642-1965del
XR_929718.1:n.3158-806_3527-1965del
XM_011518251.2:c.2191-806_2675-1965del
XM_011518252.2:c.2920-806_3404-1965del
XM_011518255.2:c.2920-806_3404-1965del
XM_017014287.1:c.2557-806_3041-1965del
XM_017014288.1:c.2410-806_2894-1965del
XM_017014289.1:c.2920-806_3404-1965del
XR_001746185.1:n.3158-806_3642-1965del
XR_929717.2:n.3158-806_3642-1965del
NM_017662.5:c.2920-806_3404-1965del
NM_001177310.2:c.2905-806_3389-1965del
NM_001177311.2:c.2905-806_3389-1965del