Canonical Allele Identifier: CA394881497

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16256959C>T (hg19) ; chr16:g.16163102C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163102C>T , CM000678.2:g.16163102C>T	GRCh38
NC_000016.9:g.16256959C>T , CM000678.1:g.16256959C>T	GRCh37
NC_000016.8:g.16164460C>T	NCBI36
NG_007558.2:g.65370G>A
NG_007558.3:g.65516G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3397G>A	ENSP00000483331.2:p.Gly1133Ser
ENST00000205557.12:c.3397G>A MANE Select	ENSP00000205557.7:p.Gly1133Ser
ENST00000640696.1:c.321-1538G>A	ENSP00000492197.1:n.321-1538G>A
ENST00000205557.11:c.3397G>A	ENSP00000205557.7:p.Gly1133Ser
ENST00000456970.6:c.3132-1538G>A	ENSP00000405002.2:n.3132-1538G>A
ENST00000622290.4:c.*606G>A	ENSP00000483331.1:n.*606G>A
NM_001171.5:c.3397G>A	NP_001162.4:p.Gly1133Ser
XM_011522479.1:c.3364G>A	XP_011520781.1:p.Gly1122Ser
XM_011522480.1:c.3055G>A	XP_011520782.1:p.Gly1019Ser
XM_011522481.1:c.3055G>A	XP_011520783.1:p.Gly1019Ser
XR_932836.1:n.3632G>A
XR_932837.1:n.3543-1538G>A
XR_932838.1:n.3543-1538G>A
XR_933133.1:n.407+259C>T
XR_933134.1:n.754+259C>T
NM_001351800.1:c.3055G>A	NP_001338729.1:p.Gly1019Ser
NR_147784.1:n.3169-1538G>A
XM_011522479.2:c.3364G>A	XP_011520781.1:p.Gly1122Ser
XM_011522481.3:c.3055G>A	XP_011520783.1:p.Gly1019Ser
XM_017023212.1:c.3229G>A	XP_016878701.1:p.Gly1077Ser
XM_017023214.1:c.3307-1538G>A	XP_016878703.1:n.3307-1538G>A
XM_024450261.1:c.3433G>A	XP_024306029.1:p.Gly1145Ser
XR_932836.2:n.3578G>A
XR_932837.3:n.3488-1538G>A
XR_932838.3:n.3488-1538G>A
NM_001171.6:c.3397G>A MANE Select	NP_001162.5:p.Gly1133Ser