Canonical Allele Identifier: CA360812194

Gene: CARINH LINC02863

Linked Data

• MyVariant Identifiers: chr5:g.131755585A>G (hg19) ; chr5:g.132419893A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419893A>G , CM000667.2:g.132419893A>G	GRCh38
NC_000005.9:g.131755585A>G , CM000667.1:g.131755585A>G	GRCh37
NC_000005.8:g.131783484A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-256A>G	ENSP00000492349.2:n.-256A>G
ENST00000638504.1:n.159A>G
ENST00000638568.2:c.-398A>G	ENSP00000491158.2:n.-398A>G
ENST00000639899.1:n.202A>G
ENST00000337752.6:c.1A>G (CARINH)	ENSP00000338228.2:p.Met1Val
ENST00000378947.7:c.1A>G (CARINH)	ENSP00000368230.3:p.Met1Val
ENST00000378953.8:c.1A>G (CARINH)	ENSP00000368236.4:p.Met1Val
ENST00000407797.5:c.1A>G (CARINH)	ENSP00000385513.1:p.Met1Val
ENST00000461203.5:n.132A>G (CARINH)
ENST00000621237.1:c.1A>G (CARINH)	ENSP00000481774.1:p.Met1Val
NR_045116.1:n.340A>G (CARINH)
NM_001207001.2:c.1A>G (CARINH)	NP_001193930.1:p.Met1Val
XR_948788.3:n.894-144T>C (LINC02863)
NR_161242.1:n.184A>G (CARINH)