Canonical Allele Identifier: CA446938289

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147510878A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131315A>C , CM000667.2:g.148131315A>C	GRCh38
NC_000005.9:g.147510878A>C , CM000667.1:g.147510878A>C	GRCh37
NC_000005.8:g.147491071A>C	NCBI36
NG_009633.1:g.72344A>C , LRG_110:g.72344A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.3021A>C MANE Select	ENSP00000256084.7:p.Pro1007=
ENST00000256084.7:c.3021A>C	ENSP00000256084.7:p.Pro1007=
ENST00000359874.7:c.3111A>C	ENSP00000352936.3:p.Pro1037=
NM_001127698.1:c.3111A>C	NP_001121170.1:p.Pro1037=
NM_006846.3:c.3021A>C , LRG_110t1:c.3021A>C	NP_006837.2:p.Pro1007=
XM_011537550.1:c.3054A>C	XP_011535852.1:p.Pro1018=
XM_011537551.1:c.3027A>C	XP_011535853.1:p.Pro1009=
XM_011537551.2:c.3027A>C	XP_011535853.1:p.Pro1009=
NM_001127698.2:c.3111A>C	NP_001121170.1:p.Pro1037=
NM_006846.4:c.3021A>C MANE Select	NP_006837.2:p.Pro1007=