Canonical Allele Identifier: CA841835385

Gene: CALN1

Linked Data

• dbSNP Id: rs1486578324
• MyVariant Identifiers: chr7:g.71388780A>C (hg19) ; chr7:g.71923795A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.71923795A>C , CM000669.2:g.71923795A>C	GRCh38
NC_000007.13:g.71388780A>C , CM000669.1:g.71388780A>C	GRCh37
NC_000007.12:g.71026716A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395275.7:c.501+99862T>G MANE Select	ENSP00000378690.2:n.501+99862T>G
ENST00000329008.9:c.375+99862T>G	ENSP00000332498.5:n.375+99862T>G
ENST00000395275.6:c.501+99862T>G	ENSP00000378690.2:n.501+99862T>G
ENST00000395276.6:c.375+99862T>G	ENSP00000378691.2:n.375+99862T>G
ENST00000431984.5:c.375+99862T>G	ENSP00000410704.1:n.375+99862T>G
NM_001017440.2:c.375+99862T>G	NP_001017440.1:n.375+99862T>G
NM_031468.3:c.501+99862T>G	NP_113656.2:n.501+99862T>G
XM_011516593.1:c.375+99862T>G	XP_011514895.1:n.375+99862T>G
XM_011516594.1:c.426+99862T>G	XP_011514896.1:n.426+99862T>G
XM_011516595.1:c.375+99862T>G	XP_011514897.1:n.375+99862T>G
XM_011516596.1:c.375+99862T>G	XP_011514898.1:n.375+99862T>G
XM_011516597.1:c.375+99862T>G	XP_011514899.1:n.375+99862T>G
XM_011516599.1:c.375+99862T>G	XP_011514901.1:n.375+99862T>G
NM_001363460.1:c.375+99862T>G	NP_001350389.1:n.375+99862T>G
XM_011516594.3:c.426+99862T>G	XP_011514896.1:n.426+99862T>G
XM_011516596.2:c.375+99862T>G	XP_011514898.1:n.375+99862T>G
XM_011516597.2:c.375+99862T>G	XP_011514899.1:n.375+99862T>G
XM_017012675.1:c.501+99862T>G	XP_016868164.1:n.501+99862T>G
XM_017012676.2:c.501+99862T>G	XP_016868165.1:n.501+99862T>G
XM_017012677.1:c.384+99862T>G	XP_016868166.1:n.384+99862T>G
XM_017012678.1:c.375+99862T>G	XP_016868167.1:n.375+99862T>G
XM_017012679.1:c.375+99862T>G	XP_016868168.1:n.375+99862T>G
XM_017012680.1:c.375+99862T>G	XP_016868169.1:n.375+99862T>G
XM_017012681.1:c.375+99862T>G	XP_016868170.1:n.375+99862T>G
XM_017012682.1:c.375+99862T>G	XP_016868171.1:n.375+99862T>G
XM_017012683.1:c.375+99862T>G	XP_016868172.1:n.375+99862T>G
NM_031468.4:c.501+99862T>G MANE Select	NP_113656.2:n.501+99862T>G
NM_001017440.3:c.375+99862T>G	NP_001017440.1:n.375+99862T>G