Canonical Allele Identifier: CA2515012998

Gene: SMC1A MIR6857

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405690_53405691insC , CM000685.2:g.53405690_53405691insC	GRCh38
NC_000023.10:g.53432622_53432623insC , CM000685.1:g.53432622_53432623insC	GRCh37
NC_000023.9:g.53449347_53449348insC	NCBI36
NG_006988.2:g.21980_21981insG , LRG_773:g.21980_21981insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1732-19_1732-18insG (SMC1A) MANE Select	ENSP00000323421.3:n.1732-19_1732-18insG
ENST00000674590.1:c.964-19_964-18insG (SMC1A)	ENSP00000502626.1:n.964-19_964-18insG
ENST00000675065.1:n.1084-19_1084-18insG (SMC1A)
ENST00000675504.1:c.1666-19_1666-18insG (SMC1A)	ENSP00000502524.1:n.1666-19_1666-18insG
ENST00000322213.8:c.1732-19_1732-18insG (SMC1A)	ENSP00000323421.3:n.1732-19_1732-18insG
ENST00000375340.10:c.1666-19_1666-18insG (SMC1A)	ENSP00000364489.7:n.1666-19_1666-18insG
NM_001281463.1:c.1666-19_1666-18insG , LRG_773t1:c.1666-19_1666-18insG (SMC1A)	NP_001268392.1:n.1666-19_1666-18insG
NM_006306.3:c.1732-19_1732-18insG , LRG_773t2:c.1732-19_1732-18insG (SMC1A)	NP_006297.2:n.1732-19_1732-18insG
NR_106916.1:n.75_76insG (MIR6857)
NM_006306.4:c.1732-19_1732-18insG (SMC1A) MANE Select	NP_006297.2:n.1732-19_1732-18insG