Canonical Allele Identifier: CA394887731

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16271419G>A (hg19) ; chr16:g.16177562G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16177562G>A , CM000678.2:g.16177562G>A	GRCh38
NC_000016.9:g.16271419G>A , CM000678.1:g.16271419G>A	GRCh37
NC_000016.8:g.16178920G>A	NCBI36
NG_007558.2:g.50910C>T
NG_007558.3:g.51056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2480C>T	ENSP00000483331.2:p.Ala827Val
ENST00000205557.12:c.2480C>T MANE Select	ENSP00000205557.7:p.Ala827Val
ENST00000205557.11:c.2480C>T	ENSP00000205557.7:p.Ala827Val
ENST00000456970.6:c.2415+1236C>T	ENSP00000405002.2:n.2415+1236C>T
ENST00000622290.4:c.2415+1236C>T	ENSP00000483331.1:n.2415+1236C>T
NM_001171.5:c.2480C>T	NP_001162.4:p.Ala827Val
XM_011522479.1:c.2447C>T	XP_011520781.1:p.Ala816Val
XM_011522480.1:c.2138C>T	XP_011520782.1:p.Ala713Val
XM_011522481.1:c.2138C>T	XP_011520783.1:p.Ala713Val
XM_011522482.1:c.2480C>T	XP_011520784.1:p.Ala827Val
XR_932836.1:n.2715C>T
XR_932837.1:n.2716C>T
XR_932838.1:n.2716C>T
NM_001351800.1:c.2138C>T	NP_001338729.1:p.Ala713Val
NR_147784.1:n.2452+1236C>T
XM_011522479.2:c.2447C>T	XP_011520781.1:p.Ala816Val
XM_011522481.3:c.2138C>T	XP_011520783.1:p.Ala713Val
XM_011522482.3:c.2480C>T	XP_011520784.1:p.Ala827Val
XM_017023212.1:c.2312C>T	XP_016878701.1:p.Ala771Val
XM_017023214.1:c.2480C>T	XP_016878703.1:p.Ala827Val
XM_024450261.1:c.2516C>T	XP_024306029.1:p.Ala839Val
XR_932836.2:n.2661C>T
XR_932837.3:n.2661C>T
XR_932838.3:n.2661C>T
NM_001171.6:c.2480C>T MANE Select	NP_001162.5:p.Ala827Val