Canonical Allele Identifier: CA394878869

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16253415A>G (hg19) ; chr16:g.16159558A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159558A>G , CM000678.2:g.16159558A>G	GRCh38
NC_000016.9:g.16253415A>G , CM000678.1:g.16253415A>G	GRCh37
NC_000016.8:g.16160916A>G	NCBI36
NG_007558.2:g.68914T>C
NG_007558.3:g.69060T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3659T>C	ENSP00000483331.2:p.Val1220Ala
ENST00000205557.12:c.3659T>C MANE Select	ENSP00000205557.7:p.Val1220Ala
ENST00000640696.1:c.473T>C	ENSP00000492197.1:p.Val158Ala
ENST00000205557.11:c.3659T>C	ENSP00000205557.7:p.Val1220Ala
ENST00000456970.6:c.3284T>C	ENSP00000405002.2:n.3284T>C
ENST00000622290.4:c.*868T>C	ENSP00000483331.1:n.*868T>C
NM_001171.5:c.3659T>C	NP_001162.4:p.Val1220Ala
XM_011522479.1:c.3626T>C	XP_011520781.1:p.Val1209Ala
XM_011522480.1:c.3317T>C	XP_011520782.1:p.Val1106Ala
XM_011522481.1:c.3317T>C	XP_011520783.1:p.Val1106Ala
XR_932836.1:n.3894T>C
XR_932837.1:n.3695T>C
XR_932838.1:n.3695T>C
XR_933134.1:n.539-223A>G
NM_001351800.1:c.3317T>C	NP_001338729.1:p.Val1106Ala
NR_147784.1:n.3321T>C
XM_011522479.2:c.3626T>C	XP_011520781.1:p.Val1209Ala
XM_011522481.3:c.3317T>C	XP_011520783.1:p.Val1106Ala
XM_017023212.1:c.3491T>C	XP_016878701.1:p.Val1164Ala
XM_024450261.1:c.3695T>C	XP_024306029.1:p.Val1232Ala
XR_932836.2:n.3840T>C
XR_932837.3:n.3640T>C
XR_932838.3:n.3640T>C
NM_001171.6:c.3659T>C MANE Select	NP_001162.5:p.Val1220Ala