Canonical Allele Identifier: CA4205514

Gene: GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30504606T>C , CM000669.2:g.30504606T>C	GRCh38
NC_000007.13:g.30544222T>C , CM000669.1:g.30544222T>C	GRCh37
NC_000007.12:g.30510747T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024051.4:c.104A>G MANE Select	NP_076956.1:p.Asn35Ser
ENST00000275428.9:c.104A>G MANE Select	ENSP00000275428.4:p.Asn35Ser
NM_001199815.1:c.104A>G	NP_001186744.1:p.Asn35Ser
NM_001199815.2:c.104A>G	NP_001186744.1:p.Asn35Ser
NM_001199816.1:c.104A>G	NP_001186745.1:p.Asn35Ser
NM_001199816.2:c.104A>G	NP_001186745.1:p.Asn35Ser
NM_001199817.1:c.104A>G	NP_001186746.1:p.Asn35Ser
NM_001199817.2:c.104A>G	NP_001186746.1:p.Asn35Ser
NM_024051.3:c.104A>G	NP_076956.1:p.Asn35Ser
NR_037669.1:n.236A>G
NR_037669.2:n.224A>G
ENST00000005374.10:c.104A>G	ENSP00000005374.6:p.Asn35Ser
ENST00000275428.8:c.104A>G	ENSP00000275428.4:p.Asn35Ser
ENST00000409144.5:c.104A>G	ENSP00000386610.1:p.Asn35Ser
ENST00000409390.5:c.104A>G	ENSP00000387235.1:p.Asn35Ser
ENST00000409436.2:c.104A>G	ENSP00000386686.1:p.Asn35Ser
ENST00000440082.5:c.104A>G	ENSP00000408015.1:p.Asn35Ser
ENST00000447901.1:c.104A>G	ENSP00000387809.1:p.Asn35Ser
ENST00000598361.4:c.-114-3925A>G	ENSP00000470615.1:n.-114-3925A>G