Canonical Allele Identifier: CA394884975

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263673A>G (hg19) ; chr16:g.16169816A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169816A>G , CM000678.2:g.16169816A>G	GRCh38
NC_000016.9:g.16263673A>G , CM000678.1:g.16263673A>G	GRCh37
NC_000016.8:g.16171174A>G	NCBI36
NG_007558.2:g.58656T>C
NG_007558.3:g.58802T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2825T>C	ENSP00000483331.2:p.Val942Ala
ENST00000205557.12:c.2825T>C MANE Select	ENSP00000205557.7:p.Val942Ala
ENST00000205557.11:c.2825T>C	ENSP00000205557.7:p.Val942Ala
ENST00000456970.6:c.2650T>C	ENSP00000405002.2:n.2650T>C
ENST00000622290.4:c.*34T>C	ENSP00000483331.1:n.*34T>C
NM_001171.5:c.2825T>C	NP_001162.4:p.Val942Ala
XM_011522479.1:c.2792T>C	XP_011520781.1:p.Val931Ala
XM_011522480.1:c.2483T>C	XP_011520782.1:p.Val828Ala
XM_011522481.1:c.2483T>C	XP_011520783.1:p.Val828Ala
XR_932836.1:n.3060T>C
XR_932837.1:n.3061T>C
XR_932838.1:n.3061T>C
NM_001351800.1:c.2483T>C	NP_001338729.1:p.Val828Ala
NR_147784.1:n.2687T>C
XM_011522479.2:c.2792T>C	XP_011520781.1:p.Val931Ala
XM_011522481.3:c.2483T>C	XP_011520783.1:p.Val828Ala
XM_017023212.1:c.2657T>C	XP_016878701.1:p.Val886Ala
XM_017023214.1:c.2825T>C	XP_016878703.1:p.Val942Ala
XM_024450261.1:c.2861T>C	XP_024306029.1:p.Val954Ala
XR_932836.2:n.3006T>C
XR_932837.3:n.3006T>C
XR_932838.3:n.3006T>C
NM_001171.6:c.2825T>C MANE Select	NP_001162.5:p.Val942Ala