Canonical Allele Identifier: CA394884981

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263674C>G (hg19) ; chr16:g.16169817C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169817C>G , CM000678.2:g.16169817C>G	GRCh38
NC_000016.9:g.16263674C>G , CM000678.1:g.16263674C>G	GRCh37
NC_000016.8:g.16171175C>G	NCBI36
NG_007558.2:g.58655G>C
NG_007558.3:g.58801G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2824G>C	ENSP00000483331.2:p.Val942Leu
ENST00000205557.12:c.2824G>C MANE Select	ENSP00000205557.7:p.Val942Leu
ENST00000205557.11:c.2824G>C	ENSP00000205557.7:p.Val942Leu
ENST00000456970.6:c.2649G>C	ENSP00000405002.2:n.2649G>C
ENST00000622290.4:c.*33G>C	ENSP00000483331.1:n.*33G>C
NM_001171.5:c.2824G>C	NP_001162.4:p.Val942Leu
XM_011522479.1:c.2791G>C	XP_011520781.1:p.Val931Leu
XM_011522480.1:c.2482G>C	XP_011520782.1:p.Val828Leu
XM_011522481.1:c.2482G>C	XP_011520783.1:p.Val828Leu
XR_932836.1:n.3059G>C
XR_932837.1:n.3060G>C
XR_932838.1:n.3060G>C
NM_001351800.1:c.2482G>C	NP_001338729.1:p.Val828Leu
NR_147784.1:n.2686G>C
XM_011522479.2:c.2791G>C	XP_011520781.1:p.Val931Leu
XM_011522481.3:c.2482G>C	XP_011520783.1:p.Val828Leu
XM_017023212.1:c.2656G>C	XP_016878701.1:p.Val886Leu
XM_017023214.1:c.2824G>C	XP_016878703.1:p.Val942Leu
XM_024450261.1:c.2860G>C	XP_024306029.1:p.Val954Leu
XR_932836.2:n.3005G>C
XR_932837.3:n.3005G>C
XR_932838.3:n.3005G>C
NM_001171.6:c.2824G>C MANE Select	NP_001162.5:p.Val942Leu