Canonical Allele Identifier: CA2574200185

Gene: CA6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957288A>T , CM000663.2:g.8957288A>T	GRCh38
NC_000001.10:g.9017347A>T , CM000663.1:g.9017347A>T	GRCh37
NC_000001.9:g.8939934A>T	NCBI36
NG_033975.1:g.16455A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.408+3A>T MANE Select	ENSP00000366662.2:n.408+3A>T
ENST00000377436.6:c.408+3A>T	ENSP00000366654.3:n.408+3A>T
ENST00000377442.3:c.228+3A>T	ENSP00000366661.2:n.228+3A>T
ENST00000377443.6:c.408+3A>T	ENSP00000366662.2:n.408+3A>T
ENST00000476083.1:n.99-1622A>T
ENST00000549778.5:c.312+3A>T	ENSP00000447108.1:n.312+3A>T
NM_001215.3:c.408+3A>T	NP_001206.2:n.408+3A>T
NM_001270500.1:c.408+3A>T	NP_001257429.1:n.408+3A>T
NM_001270501.1:c.228+3A>T	NP_001257430.1:n.228+3A>T
NM_001270502.1:c.25-1622A>T	NP_001257431.1:n.25-1622A>T
XM_011542083.1:c.420+3A>T	XP_011540385.1:n.420+3A>T
XM_011542084.1:c.420+3A>T	XP_011540386.1:n.420+3A>T
XM_011542083.3:c.420+3A>T	XP_011540385.1:n.420+3A>T
XM_011542084.3:c.420+3A>T	XP_011540386.1:n.420+3A>T
NM_001215.4:c.408+3A>T MANE Select	NP_001206.2:n.408+3A>T
NM_001270500.2:c.408+3A>T	NP_001257429.1:n.408+3A>T
NM_001270501.2:c.228+3A>T	NP_001257430.1:n.228+3A>T
NM_001270502.2:c.25-1622A>T	NP_001257431.1:n.25-1622A>T