Canonical Allele Identifier: CA394878678

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16253347G>C (hg19) ; chr16:g.16159490G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159490G>C , CM000678.2:g.16159490G>C	GRCh38
NC_000016.9:g.16253347G>C , CM000678.1:g.16253347G>C	GRCh37
NC_000016.8:g.16160848G>C	NCBI36
NG_007558.2:g.68982C>G
NG_007558.3:g.69128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3727C>G	ENSP00000483331.2:p.Pro1243Ala
ENST00000205557.12:c.3727C>G MANE Select	ENSP00000205557.7:p.Pro1243Ala
ENST00000640696.1:c.541C>G	ENSP00000492197.1:p.Pro181Ala
ENST00000205557.11:c.3727C>G	ENSP00000205557.7:p.Pro1243Ala
ENST00000456970.6:c.3352C>G	ENSP00000405002.2:n.3352C>G
ENST00000622290.4:c.*936C>G	ENSP00000483331.1:n.*936C>G
NM_001171.5:c.3727C>G	NP_001162.4:p.Pro1243Ala
XM_011522479.1:c.3694C>G	XP_011520781.1:p.Pro1232Ala
XM_011522480.1:c.3385C>G	XP_011520782.1:p.Pro1129Ala
XM_011522481.1:c.3385C>G	XP_011520783.1:p.Pro1129Ala
XR_932836.1:n.3962C>G
XR_932837.1:n.3763C>G
XR_932838.1:n.3763C>G
XR_933134.1:n.539-291G>C
NM_001351800.1:c.3385C>G	NP_001338729.1:p.Pro1129Ala
NR_147784.1:n.3389C>G
XM_011522479.2:c.3694C>G	XP_011520781.1:p.Pro1232Ala
XM_011522481.3:c.3385C>G	XP_011520783.1:p.Pro1129Ala
XM_017023212.1:c.3559C>G	XP_016878701.1:p.Pro1187Ala
XM_024450261.1:c.3763C>G	XP_024306029.1:p.Pro1255Ala
XR_932836.2:n.3908C>G
XR_932837.3:n.3708C>G
XR_932838.3:n.3708C>G
NM_001171.6:c.3727C>G MANE Select	NP_001162.5:p.Pro1243Ala