Canonical Allele Identifier: CA2573132182

Gene: HSPG2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21880742_21880743delinsCA , CM000663.2:g.21880742_21880743delinsCA	GRCh38
NC_000001.10:g.22207235_22207236delinsCA , CM000663.1:g.22207235_22207236delinsCA	GRCh37
NC_000001.9:g.22079822_22079823delinsCA	NCBI36
NG_016740.1:g.61515_61516delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374695.8:c.1911_1912delinsTG MANE Select	ENSP00000363827.3:p.Met638Val
ENST00000374695.7:c.1911_1912delinsTG	ENSP00000363827.3:p.Met638Val
NM_001291860.1:c.1914_1915delinsTG	NP_001278789.1:p.Met639Val
NM_005529.6:c.1911_1912delinsTG	NP_005520.4:p.Met638Val
XM_006710594.2:c.1962_1963delinsTG	XP_006710657.1:p.Met655Val
XM_006710595.2:c.1914_1915delinsTG	XP_006710658.1:p.Met639Val
XM_006710596.2:c.1965_1966delinsTG	XP_006710659.1:p.Met656Val
XM_006710597.2:c.1911_1912delinsTG	XP_006710660.1:p.Met638Val
XM_011541317.1:c.1965_1966delinsTG	XP_011539619.1:p.Met656Val
XM_011541318.1:c.1965_1966delinsTG	XP_011539620.1:p.Met656Val
XM_011541319.1:c.1965_1966delinsTG	XP_011539621.1:p.Met656Val
XM_011541320.1:c.1965_1966delinsTG	XP_011539622.1:p.Met656Val
XM_011541321.1:c.1965_1966delinsTG	XP_011539623.1:p.Met656Val
XM_011541322.1:c.1965_1966delinsTG	XP_011539624.1:p.Met656Val
XM_011541318.2:c.1965_1966delinsTG	XP_011539620.1:p.Met656Val
XM_017001120.1:c.2106_2107delinsTG	XP_016856609.1:p.Met703Val
XM_017001121.1:c.2055_2056delinsTG	XP_016856610.1:p.Met686Val
XM_017001122.1:c.2052_2053delinsTG	XP_016856611.1:p.Met685Val
NM_005529.7:c.1911_1912delinsTG MANE Select	NP_005520.4:p.Met638Val
NM_001291860.2:c.1914_1915delinsTG	NP_001278789.1:p.Met639Val