Canonical Allele Identifier: CA342322517

Gene: CTSS

Linked Data

• MyVariant Identifiers: chr1:g.150705622C>G (hg19) ; chr1:g.150733146C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733146C>G , CM000663.2:g.150733146C>G	GRCh38
NC_000001.10:g.150705622C>G , CM000663.1:g.150705622C>G	GRCh37
NC_000001.9:g.148972246C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897-1G>C MANE Select	ENSP00000357981.3:n.897-1G>C
ENST00000448301.7:c.669-1G>C	ENSP00000408414.2:n.669-1G>C
ENST00000472977.7:c.897-1G>C	ENSP00000475176.2:n.897-1G>C
ENST00000483930.2:c.*91-1G>C	ENSP00000475812.2:n.*91-1G>C
ENST00000607427.2:c.897-1G>C	ENSP00000475557.2:n.897-1G>C
ENST00000679512.1:c.794-1G>C	ENSP00000505113.1:n.794-1G>C
ENST00000679898.1:c.624-1G>C	ENSP00000505326.1:n.624-1G>C
ENST00000680288.1:c.747-1G>C	ENSP00000506001.1:n.747-1G>C
ENST00000680311.1:c.628-1G>C	ENSP00000505020.1:n.628-1G>C
ENST00000680471.1:c.*68-1G>C	ENSP00000506603.1:n.*68-1G>C
ENST00000680664.1:c.720-1G>C	ENSP00000506248.1:n.720-1G>C
ENST00000680931.1:c.*247-1G>C	ENSP00000504934.1:n.*247-1G>C
ENST00000681357.1:n.287-1G>C
ENST00000681444.1:c.897-1G>C	ENSP00000505359.1:n.897-1G>C
ENST00000368985.7:c.897-1G>C	ENSP00000357981.3:n.897-1G>C
ENST00000448301.6:c.747-1G>C	ENSP00000408414.1:n.747-1G>C
ENST00000472977.6:c.190-1G>C
ENST00000483930.1:c.445-1G>C	ENSP00000475812.1:n.445-1G>C
NM_001199739.1:c.747-1G>C	NP_001186668.1:n.747-1G>C
NM_004079.4:c.897-1G>C	NP_004070.3:n.897-1G>C
NM_004079.5:c.897-1G>C MANE Select	NP_004070.3:n.897-1G>C
NM_001199739.2:c.747-1G>C	NP_001186668.1:n.747-1G>C