Canonical Allele Identifier: CA2579774095
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404391_90404392delinsAT , CM000676.2:g.90404391_90404392delinsAT GRCh38
NC_000014.8:g.90870735_90870736delinsAT , CM000676.1:g.90870735_90870736delinsAT GRCh37
NC_000014.7:g.89940488_89940489delinsAT NCBI36
NG_013338.1:g.12409_12410delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.298_299delinsAT MANE Select ENSP00000349467.4:p.Tyr100Ile
ENST00000447653.8:c.190_191delinsAT ENSP00000403491.4:p.Tyr64Ile
ENST00000659177.1:c.190_191delinsAT ENSP00000499421.1:p.Tyr64Ile
ENST00000663135.1:c.190_191delinsAT ENSP00000499498.1:p.Tyr64Ile
ENST00000356978.8:c.298_299delinsAT ENSP00000349467.4:p.Tyr100Ile
ENST00000447653.7:c.301_302delinsAT ENSP00000403491.3:p.Tyr101Ile
ENST00000544280.6:c.190_191delinsAT ENSP00000442853.2:p.Tyr64Ile
ENST00000553422.1:c.178-8_178-7delinsAT ENSP00000450425.1:n.178-8_178-7delinsAT
ENST00000553542.5:c.190_191delinsAT ENSP00000450829.1:p.Tyr64Ile
ENST00000553630.1:c.191_192delinsAT ENSP00000451646.1:p.Leu64Tyr
ENST00000553964.5:n.2428_2429delinsAT
ENST00000554296.1:n.350_351delinsAT
ENST00000556721.1:n.224_225delinsAT
ENST00000557020.5:c.190_191delinsAT ENSP00000451062.1:p.Tyr64Ile
ENST00000626705.2:c.166-66_166-65delinsAT ENSP00000486402.1:n.166-66_166-65delinsAT
NM_006888.4:c.298_299delinsAT NP_008819.1:p.Tyr100Ile
XM_006720258.2:c.301_302delinsAT XP_006720321.1:p.Tyr101Ile
NM_001363669.1:c.190_191delinsAT NP_001350598.1:p.Tyr64Ile
NM_001363670.1:c.301_302delinsAT NP_001350599.1:p.Tyr101Ile
NM_006888.5:c.298_299delinsAT NP_008819.1:p.Tyr100Ile
NM_006888.6:c.298_299delinsAT MANE Select NP_008819.1:p.Tyr100Ile
NM_001363669.2:c.190_191delinsAT NP_001350598.1:p.Tyr64Ile
NM_001363670.2:c.301_302delinsAT NP_001350599.1:p.Tyr101Ile