Canonical Allele Identifier: CA237648025

Gene: CS

Linked Data

• dbSNP Id: rs977844343
• MyVariant Identifiers: chr12:g.56680667T>G (hg19) ; chr12:g.56286883T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56286883T>G , CM000674.2:g.56286883T>G	GRCh38
NC_000012.11:g.56680667T>G , CM000674.1:g.56680667T>G	GRCh37
NC_000012.10:g.54966934T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351328.8:c.43-238A>C MANE Select	ENSP00000342056.3:n.43-238A>C
ENST00000351328.7:c.43-238A>C	ENSP00000342056.3:n.43-238A>C
ENST00000542324.6:c.4-238A>C	ENSP00000440543.2:n.4-238A>C
ENST00000546930.5:c.43-238A>C	ENSP00000450403.1:n.43-238A>C
ENST00000547283.5:n.233-238A>C
ENST00000547298.5:c.-156-238A>C	ENSP00000448409.1:n.-156-238A>C
ENST00000547423.5:c.205-238A>C	ENSP00000446506.1:n.205-238A>C
ENST00000548041.5:c.43-238A>C	ENSP00000447986.1:n.43-238A>C
ENST00000548567.5:c.-156-238A>C	ENSP00000446779.1:n.-156-238A>C
ENST00000548849.5:c.43-238A>C	ENSP00000449491.1:n.43-238A>C
ENST00000549143.5:c.43-238A>C	ENSP00000449571.1:n.43-238A>C
ENST00000549221.5:c.43-3892A>C	ENSP00000448667.1:n.43-3892A>C
ENST00000549318.5:c.631-238A>C	ENSP00000446743.1:n.631-238A>C
ENST00000550044.1:n.208-263A>C
ENST00000550159.5:c.-229-263A>C	ENSP00000447346.1:n.-229-263A>C
ENST00000550655.5:c.43-238A>C	ENSP00000448172.1:n.43-238A>C
ENST00000550700.1:n.178-263A>C
ENST00000550734.5:c.-131-263A>C	ENSP00000449025.1:n.-131-263A>C
ENST00000550996.1:n.233-238A>C
ENST00000551137.5:c.-156-238A>C	ENSP00000449753.1:n.-156-238A>C
ENST00000551155.1:n.129-263A>C
ENST00000551253.5:c.-156-238A>C	ENSP00000450101.1:n.-156-238A>C
ENST00000551430.6:c.-156-238A>C	ENSP00000448166.2:n.-156-238A>C
ENST00000551441.5:n.258-238A>C
ENST00000551473.5:c.-156-238A>C	ENSP00000449427.1:n.-156-238A>C
ENST00000551936.5:c.-131-263A>C	ENSP00000450312.1:n.-131-263A>C
ENST00000551968.5:c.43-238A>C	ENSP00000447948.1:n.43-238A>C
ENST00000552222.5:c.43-238A>C	ENSP00000447582.1:n.43-238A>C
ENST00000552688.5:c.43-238A>C	ENSP00000447442.1:n.43-238A>C
NM_004077.2:c.43-238A>C	NP_004068.2:n.43-238A>C
NM_004077.3:c.43-238A>C MANE Select	NP_004068.2:n.43-238A>C