Canonical Allele Identifier: CA338184671

Gene: CA6

Linked Data

• MyVariant Identifiers: chr1:g.9017217C>T (hg19) ; chr1:g.8957158C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8957158C>T , CM000663.2:g.8957158C>T	GRCh38
NC_000001.10:g.9017217C>T , CM000663.1:g.9017217C>T	GRCh37
NC_000001.9:g.8939804C>T	NCBI36
NG_033975.1:g.16325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377443.7:c.281C>T MANE Select	ENSP00000366662.2:p.Thr94Ile
ENST00000377436.6:c.281C>T	ENSP00000366654.3:p.Thr94Ile
ENST00000377442.3:c.101C>T	ENSP00000366661.2:p.Thr34Ile
ENST00000377443.6:c.281C>T	ENSP00000366662.2:p.Thr94Ile
ENST00000476083.1:n.99-1752C>T
ENST00000549778.5:c.185C>T	ENSP00000447108.1:p.Thr62Ile
NM_001215.3:c.281C>T	NP_001206.2:p.Thr94Ile
NM_001270500.1:c.281C>T	NP_001257429.1:p.Thr94Ile
NM_001270501.1:c.101C>T	NP_001257430.1:p.Thr34Ile
NM_001270502.1:c.25-1752C>T	NP_001257431.1:n.25-1752C>T
XM_011542083.1:c.293C>T	XP_011540385.1:p.Thr98Ile
XM_011542084.1:c.293C>T	XP_011540386.1:p.Thr98Ile
XM_011542083.3:c.293C>T	XP_011540385.1:p.Thr98Ile
XM_011542084.3:c.293C>T	XP_011540386.1:p.Thr98Ile
NM_001215.4:c.281C>T MANE Select	NP_001206.2:p.Thr94Ile
NM_001270500.2:c.281C>T	NP_001257429.1:p.Thr94Ile
NM_001270501.2:c.101C>T	NP_001257430.1:p.Thr34Ile
NM_001270502.2:c.25-1752C>T	NP_001257431.1:n.25-1752C>T